Medical Device Manufacturer · US , Walker , MI

Diversied P.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1983
1
Total
1
Cleared
0
Denied

Diversied P.A. has 1 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 1 cleared submissions from 1983 to 1983. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Diversied P.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Diversied P.A.
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