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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
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EUDAMED SRN
—
FDA FEI Number
3020115
DUNS Number
—

Catalogue (436)

Page 1 of 9
DeviceModel / ReferenceRegistriesClassStatus
8.2mhz Adult Flt Probe 841/842 832-7822-21
FDA UDI
Class IIActive
2.10mhz Ob Probe 641 832-7210-21
FDA UDI
Class IIActive
9.9mhz Adult Flat Probe 832-3990-11
FDA UDI
Class IIActive
4.3mhz Pencil Probe 832-1430-11
FDA UDI
Class IIActive
4.1mhz Pencil Probe 10' 832-1410-41
FDA UDI
Class IIActive
2.25mhz Precordial Probe 832-5225-12
FDA UDI
Class IIActive
9.6mhz Adult Flat Probe 10' 832-3960-41
FDA UDI
Class IIActive
9.4mhz Adult Fl Probe 841/842 832-7942-21
FDA UDI
Class IIActive
9.2mhz Adult Flt Probe 841/842 832-7922-21
FDA UDI
Class IIActive
9.3mhz Skny Pen Probe 10' 832-2930-41
FDA UDI
Class IIActive
5mhz Pencil Probe 841/842 832-7500-21
FDA UDI
Class IIActive
9.4MHZ Pencil Probe 7FT Contoured 832-1940-33
FDA UDI
Class IIActive
Doppler 811-Bts 24v For Pmes 811-BTS 24V NV
FDA UDI
Class IIActive
3.9mhz Pencil Probe 10' 832-1390-41
FDA UDI
Class IIActive
8.4mhz Pencil Probe 10' 832-1840-41
FDA UDI
Class IIActive
8.3mhz Infant Flat Probe 832-4830-11
FDA UDI
Class IIActive
9.3mhz Microvascular Probe 832-1934-11
FDA UDI
Class IIActive
7.9mhz Pencil Probe 841/842 832-7791-21
FDA UDI
Class IIActive
811-Bl 24v Foreign & Domestic 811-BL 24V 800C
FDA UDI
Class IIActive
8.9mhz Pencil Probe 841/842 832-7891-21
FDA UDI
Class IIActive
2.25mhz Ob Probe 832-6225-11
FDA UDI
Class IIActive
9.4mhz Pencil Probe 7' 832-1940-31
FDA UDI
Class IIActive
4.1mhz Pencil Probe Shielded 832-1410-12
FDA UDI
Class IIActive
4.0mhz Pencil Probe 832-1400-11
FDA UDI
Class IIActive
8.4mhz Infant Flat Probe 832-4840-11
FDA UDI
Class IIActive
9.4mhz Skny Pen Probe 7' 832-2940-31
FDA UDI
Class IIActive
8.2mhz Adult Flat Probe 841-A 832-3820-21
FDA UDI
Class IIActive
9.4mhz Pencil Probe 832-1940-11
FDA UDI
Class IIActive
4.4mhz Pencil Probe 832-1440-11
FDA UDI
Class IIActive
8.0mhz Skny Pen Probe 841-A 832-2800-21
FDA UDI
Class IIActive
9.5mhz Pencil Probe Shld 832-1950-12
FDA UDI
Class IIActive
9.6mhz Pencil Probe 832-1960-11
FDA UDI
Class IIActive
8.5mhz Pencil Probe 832-1850-11
FDA UDI
Class IIActive
8.6mhz Pencil Probe 7' 832-1860-31
FDA UDI
Class IIActive
9.2mhz Skny Pen Probe 832-2920-11
FDA UDI
Class IIActive
4.2mhz Pencil Probe 7' 832-1420-31
FDA UDI
Class IIActive
811-Bl 24v Foreign & Domestic 811-BL 24V 901C
FDA UDI
Class IIActive
9.5mhz Infant Flat Probe 832-4950-11
FDA UDI
Class IIActive
9.0mhz Pencil Probe 7' 832-1900-31
FDA UDI
Class IIActive
8.3mhz Pencil Probe 841/842 832-7831-21
FDA UDI
Class IIActive
9.5mhz Pencil Probe 841/842 832-7951-21
FDA UDI
Class IIActive
2.15mhz Ob Probe 832-6215-11
FDA UDI
Class IIActive
8.0mhz Adult Flat Probe 841-A 832-3800-21
FDA UDI
Class IIActive
8.4mhz Skny Pen Probe 832-2840-11
FDA UDI
Class IIActive
9.0mhz Skny Pen Probe 832-2900-11
FDA UDI
Class IIActive
8.1mhz Skny Pen Probe 832-2810-11
FDA UDI
Class IIActive
2.15mhz Precordial Probe 832-5215-12
FDA UDI
Class IIActive
9.2mhz Pencil Probe 832-1920-11
FDA UDI
Class IIActive
8.3mhz Pencil Probe 841-A 832-1830-21
FDA UDI
Class IIActive
18-B Refurb. Ir Remote Rec. 300-0277-25
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.