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PARKS MEDICAL ELECTRONICS, INC.

Last updated September 17, 2026

Information

Country: US
Address: 19460 SW SHAW ST, ALOHA, OR, 97007
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3020115
DUNS Number: —

Catalogue (436)

Page 5 of 9

Device	Model / Reference	Registries	Class	Status
9.8mhz Infant Fl Probe 841/842	832-7983-21	FDA UDI	Class II	Active
8.9mhz Adult Flat Probe	832-3890-11	FDA UDI	Class II	Active
8.1mhz Adult Flt Probe 841/842	832-7812-21	FDA UDI	Class II	Active
2100-Sx & 3100-B Remote Charg-	300-0314-01	FDA UDI	Class II	Active
8.9mhz Pencil Probe	832-1890-11	FDA UDI	Class II	Active
8.8mhz Infant Flat Probe	832-4880-11	FDA UDI	Class II	Active
8.9mhz Skny Pen Probe 841-A	832-2890-21	FDA UDI	Class II	Active
811-B 24v Nv Domestic(un) Sale	811-B 24V NV D	FDA UDI	Class II	Active
8.7mhz Pencil Probe	832-1870-11	FDA UDI	Class II	Active
3.9mhz Pencil Probe 7'	832-1390-31	FDA UDI	Class II	Active
9.6mhz Skny Pen Probe	832-2960-11	FDA UDI	Class II	Active
8.0mhz Microvascular Probe	832-1804-11	FDA UDI	Class II	Active
8.3mhz Pencil Probe 840	832-7830-01	FDA UDI	Class II	Active
8.1MHz Pencil Probe 7 Foot ODU connector	832-1811-01	FDA UDI	Class II	Active
5.2mhz Pencil Probe 7'	832-1520-31	FDA UDI	Class II	Active
Refurbished 2100-Sx/3100-B Ir	301-0314-00	FDA UDI	Class II	Active
4.3mhz Pencil Probe 7'	832-1430-31	FDA UDI	Class II	Active
Doppler 811-Bts 24v In 901 C/C	811-BTS 24V 901	FDA UDI	Class II	Active
PPG Probe 6FT 3IN, Red Housing	832-8000-10	FDA UDI	Class II	Active
9.8 Mhz Pencil Probe 840	832-7980-01	FDA UDI	Class II	Active
8.1mhz Adult Flat Probe 841-A	832-3810-21	FDA UDI	Class II	Active
8.5mhz Skny Pen Probe	832-2850-11	FDA UDI	Class II	Active
5.0mhz Pencil Probe 10'	832-1500-41	FDA UDI	Class II	Active
9.6mhz Pencil Probe 841/842	832-7961-21	FDA UDI	Class II	Active
9.1MHz SKINNY PENCIL 7'	832-2910-31	FDA UDI	Class II	Active
Probe, 8.3 Skinny Pencil 10 Ft	832-2830-41	FDA UDI	Class II	Active
9.7mhz Pencil Probe 841/842	832-7971-21	FDA UDI	Class II	Active
8.8mhz Pencil Probe 840	832-7880-01	FDA UDI	Class II	Active
9.1MHz Pencil Probe 7 Foot ODU connector	832-1911-01	FDA UDI	Class II	Active
8.0mhz Pencil Probe 840	832-7800-01	FDA UDI	Class II	Active
8.6mhz Microvascular Probe	832-1864-11	FDA UDI	Class II	Active
Doppler Model 909	909(F)	FDA UDI	Class II	Active
Doppler 811-Bts 24v In 800 C/C	811-BTS 24V 800	FDA UDI	Class II	Active
Doppler Model 915-Bl	915BL(F)	FDA UDI	Class II	Active
8.1mhz Pencil Probe Shld 7'	832-1810-32	FDA UDI	Class II	Active
Pocket Doppler Model 840	840(F)	FDA UDI	Class II	Active
Doppler Model 811-Bts	811-BTS(F)	FDA UDI	Class II	Active
8.3mhz Pencil Probe	832-1830-11	FDA UDI	Class II	Active
Final Assy 2100-Remote 18-Br	300-0302-01	FDA UDI	Class II	Active
Refurbished 19-B Ir Remote Receiver	301-0376-00	FDA UDI	Class II	Active
9.9mhz Pencil Probe 10'	832-1990-41	FDA UDI	Class II	Active
8.2mhz Pencil Probe 840	832-7820-01	FDA UDI	Class II	Active
8.6mhz Pencil Probe 10'	832-1860-41	FDA UDI	Class II	Active
2.30mhz Ob Probe	832-6230-11	FDA UDI	Class II	Active
8.0mhz Skny Pen Probe 7'	832-2800-31	FDA UDI	Class II	Active
2.20mhz Ob Probe	832-6220-11	FDA UDI	Class II	Active
4.3mhz Pencil Probe 10'	832-1430-41	FDA UDI	Class II	Active
915-Bl 24v In 800 Carry Case	915-BL 24V 800C	FDA UDI	Class II	Active
9.3mhz Pencil Probe 841/842	832-7931-21	FDA UDI	Class II	Active
9.4MHz Pencil Probe 7 Foot ODU connector	832-1941-01	FDA UDI	Class II	Active

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FDA Recalls (5)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 8, 2012	Z-0443-2013	—	terminated	Parks Medical Electronics, Inc. was made aware of two incidents where an air supply tube from their PARKS PVR unit was inadvertently connected to an IV in the patient's arm instead of into the blood pressure cuff.
Nov 8, 2007	Z-0672-2008	—	terminated	Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter.
Nov 8, 2007	Z-0670-2008	—	terminated	Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter.
Nov 8, 2007	Z-0671-2008	—	terminated	Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter.
Nov 8, 2007	Z-0673-2008	—	terminated	Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter.