Medical Device Manufacturer · US , Woodinville , WA

Pro-Tech Services, Inc. - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Pro-Tech Services, Inc. has 6 FDA 510(k) cleared medical devices. Based in Woodinville, US.

Historical record: 6 cleared submissions from 1994 to 2005. Primary specialty: Anesthesiology.

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

Pro-Tech Services, 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-Tech Services, Inc.

7 devices

1-7 of 7