Intertape Polymer, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intertape Polymer, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Intertape Polymer Inc., Type 1 Bismuth Process Indicator Steam Sterilization Tape
1
Total
1
Cleared
0
Denied
Intertape Polymer, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Intertape Polymer, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Highpower Validation Testing & Lab Service'S, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Intertape Polymer, Inc.
1 devices