Medical Device Manufacturer · US , Washington , DC

Procare C/O Wiley, Rein & Fielding - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1987
1
Total
1
Cleared
0
Denied

Procare C/O Wiley, Rein & Fielding has 1 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Procare C/O Wiley, Rein & Fielding Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Procare C/O Wiley, Rein & Fielding

1 devices
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