Technetics, Inc.
Country not established
- Devices
- 1
What Technetics, Inc. makes
Technetics, Inc. manufactures the POLYCORD II, a medical device designed for vascular applications, likely as a catheter or graft used in coronary or peripheral vascular procedures.
The POLYCORD II is classified as a Class II device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Polycord Ii Ref K880303
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technetics, Inc. have in the registry?
The registry currently lists 1 device for Technetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technetics, Inc.'s devices?
Among its 1 most recently registered device, Technetics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Technetics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Technetics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technetics, Inc. in the registry?
The most recently registered devices listed for Technetics, Inc. include POLYCORD II.