Medical Device Manufacturer · US , Sturbridge , MA

Netoptix Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1997

Total

Cleared

Denied

Netoptix Corp. has 4 FDA 510(k) cleared medical devices. Based in Sturbridge, US.

Historical record: 4 cleared submissions from 1997 to 1998. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Netoptix Corp. Filter by specialty or product code using the sidebar.

Netoptix Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Netoptix Corp.

4 devices

1-4 of 4