Medical Device Manufacturer · US , Natick , MA

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

3 submissions · 3 cleared · Since 2002

Total

Cleared

Denied

Precision Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Natick, US.

Historical record: 3 cleared submissions from 2002 to 2003. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Precision Systems, Inc. Filter by specialty or product code using the sidebar.

Precision Systems, Inc. is one of 24901 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Precision Systems, Inc.

3 devices

1-3 of 3