Medical Device Manufacturer · US , Irvine , CA

Pro-Tec Containers, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1989

Total

Cleared

Denied

Pro-Tec Containers, Inc. has 6 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 6 cleared submissions from 1989 to 1994. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Pro-Tec Containers, Inc. Filter by specialty or product code using the sidebar.

Pro-Tec Containers, 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 - Pro-Tec Containers, Inc.

6 devices

1-6 of 6