Medical Device Manufacturer · US , Woodinville , WA

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

7 submissions · 6 cleared · Since 1992

Total

Cleared

Denied

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

Historical record: 6 cleared submissions from 1992 to 1995. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Pro-Tech, Inc.

7 devices

1-7 of 7