Medical Device Manufacturer · US , Wilkes Barre Twp , PA

Ken Kemmerer - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

Ken Kemmerer has 2 FDA 510(k) cleared medical devices. Based in Wilkes Barre Twp, US.

Historical record: 2 cleared submissions from 1994 to 1996. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Ken Kemmerer Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ken Kemmerer

2 devices
1-2 of 2
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