Medical Device Manufacturer · US , Columbus , IN

Kestrel - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1990

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kestrel Ophthalmic ✕

3 devices

1-3 of 3

Cleared May 31, 1990

KESTREL LENS CASE (208-12NT POLYSTYRENE)

Ophthalmic · 44d

Cleared Jan 30, 1990

KESTREL LENS CASE 731H-893S/P-1700-2611

Ophthalmic · 27d

Cleared Jan 30, 1990

KESTREL LENS CASE 1543-893S/P-1700-2611

Ophthalmic · 27d