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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 6 of 9

Device	Model / Reference	Registries	Class	Status
Doppler Model 1052-C W/Ppg	1052-C	FDA UDI	Class II	Active
8.7mhz Pencil Probe 840	832-7870-01	FDA UDI	Class II	Active
9.5mhz Skny Pen Probe	832-2950-11	FDA UDI	Class II	Active
9.7mhz Avian Infant	832-0970-11	FDA UDI	Class II	Active
9.0mhz Skny Pen Probe 7'	832-2900-31	FDA UDI	Class II	Active
Pocket Doppler Model 841-A	841-A	FDA UDI	Class II	Active
Doppler Model 841-A W/Inf	841-A CE-2	FDA UDI	Class II	Active
Doppler Model 1059-C W/Ppg	1059-C(F)	FDA UDI	Class II	Active
5.0mhz Pencil Probe	832-1500-11	FDA UDI	Class II	Active
8.2mhz Infant Flat 10'	832-4820-41	FDA UDI	Class II	Active
2.30mhz Precordial Probe	832-5230-12	FDA UDI	Class II	Active
2.10mhz Precordial Probe	832-5210-12	FDA UDI	Class II	Active
Doppler Model 812	812-1	FDA UDI	Class II	Active
8.6mhz Infant Flat Probe	832-4860-11	FDA UDI	Class II	Active
2100-Sx2 Final Feature Item	2100-SX2 FFI	FDA UDI	Class II	Active
9.7mhz Skny Pen Probe 7'	832-2970-31	FDA UDI	Class II	Active
8.9mhz Pencil Probe 10'	832-1890-41	FDA UDI	Class II	Active
Refurbished 18-Br Remote	301-0302-00	FDA UDI	Class II	Active
8.2MHz SKNY PEN PROBE 10'	832-2820-41	FDA UDI	Class II	Active
8.7mhz Microvascular Probe	832-1874-11	FDA UDI	Class II	Active
2.00mhz Ob Probe 641	832-7200-21	FDA UDI	Class II	Active
9.8mhz Pencil Probe 10'	832-1980-41	FDA UDI	Class II	Active
8.2mhz Infant Fl Probe 841/842	832-7823-21	FDA UDI	Class II	Active
9.3mhz Adult Flat Probe Shld	832-3930-12	FDA UDI	Class II	Active
9.3mhz Pencil Probe 7'	832-1930-31	FDA UDI	Class II	Active
9.2mhz Infant Flat Probe	832-4920-11	FDA UDI	Class II	Active
8.8mhz Pencil Probe 10'	832-1880-41	FDA UDI	Class II	Active
4.0mhz Pencil Probe 7'	832-1400-31	FDA UDI	Class II	Active
8.7mhz Infant Flat Probe	832-4870-11	FDA UDI	Class II	Active
8.6mhz Skny Pen Probe	832-2860-11	FDA UDI	Class II	Active
8.1mhz Pencil Probe	832-1810-11	FDA UDI	Class II	Active
9.3mhz Microvascular Probe 7'	832-1934-31	FDA UDI	Class II	Active
9.3mhz Avian Infant	832-0930-11	FDA UDI	Class II	Active
9.6mhz Skny Pen Probe 10'	832-2960-41	FDA UDI	Class II	Active
Shielded Ppg Probe 6'3"	832-8001-00	FDA UDI	Class II	Active
9.7MHz Pencil Probe 7 Foot ODU connector	832-1971-01	FDA UDI	Class II	Active
5.1mhz Pencil Probe 840	832-7510-01	FDA UDI	Class II	Active
9.4mhz Pencil Probe 10'	832-1940-41	FDA UDI	Class II	Active
9.1mhz Pencil Probe	832-1910-11	FDA UDI	Class II	Active
8.5mhz Microvascular Probe	832-1854-11	FDA UDI	Class II	Active
8.9mhz Adult Flat Probe 7'	832-3890-31	FDA UDI	Class II	Active
8.2mhz Microvascular Probe	832-1824-11	FDA UDI	Class II	Active
8.6mhz Adult Flat Probe	832-3860-11	FDA UDI	Class II	Active
8.3mhz Infant Fl Probe 841/842	832-7833-21	FDA UDI	Class II	Active
8.2mhz Pencil Probe 10'	832-1820-41	FDA UDI	Class II	Active
8.8mhz Pencil Probe 841-A	832-1880-21	FDA UDI	Class II	Active
9.4mhz Pencil Probe Shielded	832-1940-12	FDA UDI	Class II	Active
9.0mhz Infant Flat Probe	832-4900-11	FDA UDI	Class II	Active
Doppler 811-Bl 24v Domestic	811-BL 24V	FDA UDI	Class II	Active
9.1mhz Adult Flat Probe 7'	832-3910-31	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.