Medical Device Manufacturer · US , Lowell , MA

Usfilter/Ionpure, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1998

Total

Cleared

Denied

Usfilter/Ionpure, Inc. has 3 FDA 510(k) cleared medical devices. Based in Lowell, US.

Historical record: 3 cleared submissions from 1998 to 2003. Primary specialty: Gastroenterology & Urology.

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

Usfilter/Ionpure, Inc. 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 - Usfilter/Ionpure, Inc.

3 devices

1-3 of 3