Medical Device Manufacturer · US , Kenosha , WI

Beere Precision Medical Instruments, Kmedic, Telef - FDA 510(k) Clear...

1 submissions · 1 cleared · Since 2009
1
Total
1
Cleared
0
Denied

Beere Precision Medical Instruments, Kmedic, Telef has 1 FDA 510(k) cleared medical devices. Based in Kenosha, US.

Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Beere Precision Medical Instruments, Kmedic, Telef Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Beere Precision Medical Instruments, Kmedic, Telef

1 devices
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