Medical Device Manufacturer · US , MI

Precision Instruments, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1980

4

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Precision Instruments, Inc. Ophthalmic ✕

3 devices

1-3 of 3

Cleared Jan 20, 1987

BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON

Ophthalmic · 64d

Cleared Mar 25, 1986

BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA

Ophthalmic · 33d

Cleared Oct 05, 1984

RING SUPPORTED TREPHINE FOR CORNEA TRANS

Ophthalmic · 63d