Impax Technology, Inc. is one of 344 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Impax Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DDS, DS3000, RS3000, CS5000, OT3000, IS3000, RS5000, CD3000, US3000, (AMONGST OTHER NAMES)
1
Total
1
Cleared
0
Denied
Impax Technology, Inc. has 1 FDA 510(k) cleared medical devices. Based in Waterloo, Ontario, CA.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Impax Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Impax Technology, Inc.
1 devices