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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 2 of 9
DeviceModel / ReferenceRegistriesClassStatus
8.1 MHz Pencil Probe 7FT Contoured 832-0810-33
FDA UDI
Class IIActive
9.3mhz Pencil Probe 10' 832-1930-41
FDA UDI
Class IIActive
8.3mhz Adult Flat Probe 841-A 832-3830-21
FDA UDI
Class IIActive
9.2mhz Pencil Probe 10' 832-1920-41
FDA UDI
Class IIActive
Doppler 811-Bts 24v Domestic 811-BTS 24V
FDA UDI
Class IIActive
8.3mhz Adult Fl Probe 841/842 832-7832-21
FDA UDI
Class IIActive
9.5mhz Adult Flat Probe 832-3950-11
FDA UDI
Class IIActive
5.0mhz Pencil Probe 7' 832-1500-31
FDA UDI
Class IIActive
9.9mhz Infant Flat Probe 832-4990-11
FDA UDI
Class IIActive
9.1mhz Pencil Probe 10' 832-1910-41
FDA UDI
Class IIActive
8.1mhz Skny Pencil Probe 832-2810-21
FDA UDI
Class IIActive
8.1mhz Microvascular Probe 832-1814-11
FDA UDI
Class IIActive
9.6mhz Adult Flat Probe 832-3960-11
FDA UDI
Class IIActive
9.7mhz Adult Flat Probe 10' 832-3970-41
FDA UDI
Class IIActive
9.1mhz Infant Flat Probe 832-4910-11
FDA UDI
Class IIActive
8.3mhz Adult Flat Probe 832-3830-11
FDA UDI
Class IIActive
8.5mhz Pencil 841/842 832-7851-21
FDA UDI
Class IIActive
9.6mhz Infant Flat Probe 832-4960-11
FDA UDI
Class IIActive
9.6mhz Microvascular Probe 832-1964-11
FDA UDI
Class IIActive
812 Foreign 220v Sales Kit 812 (F) 220V
FDA UDI
Class IIActive
8.0mhz Infant Flat Probe 7' 832-4800-31
FDA UDI
Class IIActive
2.25mhz Ob Probe 641-A 832-6225-21
FDA UDI
Class IIActive
9.8mhz Infant Flat Probe 10' 832-4980-41
FDA UDI
Class IIActive
9.6mhz Skny Pen Probe 7' 832-2960-31
FDA UDI
Class IIActive
9.5mhz Pencil Probe 10' 832-1950-41
FDA UDI
Class IIActive
9.0mhz Adult Flat Probe 841-A 832-3900-21
FDA UDI
Class IIActive
Pocket Doppler Model 841-A 841-A (F)
FDA UDI
Class IIActive
8.0mhz Infant Fl Probe 841/842 832-7803-21
FDA UDI
Class IIActive
8.6mhz Pencil Probe 841/842 832-7861-21
FDA UDI
Class IIActive
5.3mhz Pencil Probe 10' 832-1530-41
FDA UDI
Class IIActive
811-Bl 24v Foreign & Domestic 811-BL 24V NV
FDA UDI
Class IIActive
2.00mhz Precordial Probe 832-5200-12
FDA UDI
Class IIActive
Ce Doppler Model 841-A W/Pen 841-A
FDA UDI
Class IIActive
Doppler Model 812 Foreign 120v 812-1-F 120V
FDA UDI
Class IIActive
Vas./Ob Doppler Model 917 24v 917 24V (F)
FDA UDI
Class IIActive
Doppler Model 810-A Kit 810-A
FDA UDI
Class IIActive
3.9MHz Pencil Probe 7 Foot ODU connector 832-1391-01
FDA UDI
Class IIActive
8.1mhz Infant Flat Probe 832-4810-11
FDA UDI
Class IIActive
9.1mhz Skny Pencil 10' 832-2910-41
FDA UDI
Class IIActive
8.1mhz Pencil Probe 841/842 832-7811-21
FDA UDI
Class IIActive
5.1mhz Pencil Probe 7' 832-1510-31
FDA UDI
Class IIActive
8.3mhz Adult Flat Probe 7' 832-3830-31
FDA UDI
Class IIActive
9.3mhz Skny Pen Probe 832-2930-11
FDA UDI
Class IIActive
2.20mhz Ob Probe 641 832-7220-21
FDA UDI
Class IIActive
8.9mhz Adult Flat Probe 841-A 832-3890-21
FDA UDI
Class IIActive
8.6mhz Pencil Probe 832-1860-11
FDA UDI
Class IIActive
9.4mhz Infant Flat Probe 832-4940-11
FDA UDI
Class IIActive
3.9mhz Pencil Probe 832-1390-11
FDA UDI
Class IIActive
8.0mhz Adult Flat Probe 832-3800-11
FDA UDI
Class IIActive
8.7mhz Skny Pen Probe 832-2870-11
FDA UDI
Class IIActive

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Authorities

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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.