Precision Optics Corp. is one of 24536 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Optics Corp. - FDA 510(k) Cleared Devices
Recent clearances: PRECISION OPTICS CORPORATION VIDEO OPHTHALMOSCOPE, MODEL 2500-VOS, POC ENT ENDOSCOPE - SINUSCOPE, POC ARTHROSCOPE AND ACCESSORIES
3
Total
3
Cleared
0
Denied
Precision Optics Corp. has 3 FDA 510(k) cleared medical devices. Based in Gardner, US.
Historical record: 3 cleared submissions from 1995 to 2006.
Browse the FDA 510(k) cleared devices submitted by Precision Optics Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Precision Optics Corp.
3 devices