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PARKS MEDICAL ELECTRONICS, INC.

US

Last updated September 17, 2026

Information

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

Catalogue (436)

Page 7 of 9
DeviceModel / ReferenceRegistriesClassStatus
8.1mhz Infant Flat Probe Shld 832-4810-12
FDA UDI
Class IIActive
8.9mhz Adult Flat Probe 10' 832-3890-41
FDA UDI
Class IIActive
9.0mhz Pencil Probe 832-1900-11
FDA UDI
Class IIActive
8.1mhz Pencil Probe 841-A 832-1810-21
FDA UDI
Class IIActive
2.10mhz Ob Probe 832-6210-11
FDA UDI
Class IIActive
8.9mhz Pencil Probe 7' 832-1890-31
FDA UDI
Class IIActive
8.7MHZ Pencil Probe 7FT Contoured 832-1870-33
FDA UDI
Class IIActive
9.3mhz Pencil Probe Shielded 832-1930-12
FDA UDI
Class IIActive
8.2mhz Pencil Probe 841-A 832-1820-21
FDA UDI
Class IIActive
Doppler Model 810-A 810-A(F)
FDA UDI
Class IIActive
Doppler Model 812 In 800 C/C 812-1-800 CC
FDA UDI
Class IIActive
9.3mhz Infant Flat Probe 832-4930-11
FDA UDI
Class IIActive
8.5mhz Avian Infant 832-0850-11
FDA UDI
Class IIActive
4.2mhz Pencil Probe 832-1420-11
FDA UDI
Class IIActive
9.3mhz Pencil Probe 832-1930-11
FDA UDI
Class IIActive
811-B 24v Kit 901cc Pmes 811-B24V 901 NV
FDA UDI
Class IIActive
8.3mhz Pencil Probe 7' 832-1830-31
FDA UDI
Class IIActive
9.3mhz Adult Flat Probe 832-3930-11
FDA UDI
Class IIActive
9.9mhz Pencil Probe 7' 832-1990-31
FDA UDI
Class IIActive
8.3MHz Pencil Probe 7 Foot ODU connector 832-1831-01
FDA UDI
Class IIActive
811-Bl 24v Sales Kit W/901cc 811-BL 24V 901
FDA UDI
Class IIActive
19-B Ir Remote Receiver 300-0376-00
FDA UDI
Class IIActive
9.2mhz Pencil Probe Shielded 832-1920-12
FDA UDI
Class IIActive
8.3mhz Pencil Probe 10' 832-1830-41
FDA UDI
Class IIActive
8.2mhz Pencil Probe 832-1820-11
FDA UDI
Class IIActive
Doppler Model 841-A Nevada 841-A NV
FDA UDI
Class IIActive
811-B 24v Domestic (un) Sales 811-B 24V
FDA UDI
Class IIActive
8.2mhz Pencil Probe 841/842 832-7821-21
FDA UDI
Class IIActive
9.8mhz Pencil Probe 832-1980-11
FDA UDI
Class IIActive
8.7MHz Pencil Probe 7 Foot ODU connector 832-1871-01
FDA UDI
Class IIActive
8.4mhz Pencil Probe 841-A 832-1840-21
FDA UDI
Class IIActive
9.1mhz Adult Flat Probe 10' 832-3910-41
FDA UDI
Class IIActive
9.1mhz Pencil Probe 7' 832-1910-31
FDA UDI
Class IIActive
5.1mhz Pencil Probe 10' 832-1510-41
FDA UDI
Class IIActive
9.0mhz Pencil Probe 841-A 832-1900-21
FDA UDI
Class IIActive
Probe Infant Flat 9.1mhz 7ft 832-4910-31
FDA UDI
Class IIActive
9.4mhz Skny Pen Probe 832-2940-11
FDA UDI
Class IIActive
8.8mhz Pencil Probe 7' 832-1880-31
FDA UDI
Class IIActive
8.2mhz Avian Infant 832-0820-11
FDA UDI
Class IIActive
9.2mhz Microvascular Probe 832-1924-11
FDA UDI
Class IIActive
9.0mhz Adult Flat Probe 10' 832-3900-41
FDA UDI
Class IIActive
2.15mhz Ob Probe 641 832-7215-21
FDA UDI
Class IIActive
9.1mhz Microvascular Probe 832-1914-11
FDA UDI
Class IIActive
2.20mhz Precordial Probe 832-5220-12
FDA UDI
Class IIActive
9.7mhz Pencil Probe Shld 832-1970-12
FDA UDI
Class IIActive
8.8mhz Pencil Probe 841/842 832-7881-21
FDA UDI
Class IIActive
9.6mhz Pencil Probe 7' 832-1960-31
FDA UDI
Class IIActive
7.8mhz Pencil Probe 841-A 832-1780-21
FDA UDI
Class IIActive
9.9mhz Pencil Probe 841-A 832-1990-21
FDA UDI
Class IIActive
8.1 Mhz Skny Pen Probe 10' 832-2810-41
FDA UDI
Class IIActive

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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.

DateRecall No.ClassStatusReason
Aug 8, 2012Z-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, 2007Z-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, 2007Z-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, 2007Z-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, 2007Z-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.