Precision Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Instruments, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Precision Instruments, Inc. has 3 FDA 510(k) cleared medical devices. Based in US.
Historical record: 3 cleared submissions from 1980 to 1987. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Precision Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Precision Instruments, Inc.
4 devices
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
Cleared
Oct 03, 1980
HESSBURG-BFRRON TREPHINE
General & Plastic Surgery
84d