Pan-Tech Research, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pan-Tech Research, Inc. makes
Pan-Tech Research, Inc. manufactures the INTRA-ALERT, a medical device designed for intra-operative monitoring, and the VEIN-SHIELD, a protective barrier used during vascular procedures to reduce complications.
The company’s portfolio includes devices classified under FDA Class I and Class II, with products listed via the 510(k) pathway. These devices are regulated under the US FDA and are based in the United States.
Catalogue
Intra-Alert Ref K781297
Regimes: 510(k) Registry: 510(k)Vein-Shield Ref K820759
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pan-Tech Research, Inc. have in the registry?
The registry currently lists 2 devices for Pan-Tech Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pan-Tech Research, Inc.'s devices?
Among its 2 most recently registered devices, Pan-Tech Research, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pan-Tech Research, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pan-Tech Research, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pan-Tech Research, Inc. in the registry?
The most recently registered devices listed for Pan-Tech Research, Inc. include INTRA-ALERT and VEIN-SHIELD.