Medical Device Manufacturer · US , MI

Precision Instruments, Inc.

4 submissions · 3 cleared · Since 1980
4
Total
3
Cleared
0
Denied

Precision Instruments, Inc. — FDA 510(k) Submissions

Precision Instruments, Inc. has submitted 4 FDA 510(k) premarket notifications since 1980, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Trephine, Manual, Ophthalmic, Knife, Surgical . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
Filters
Filter by Specialty
All4 Ophthalmic 3 General & Plastic Surgery 1