Philip Munsterman Tan, Inc.
Country not established
- Devices
- 1
What Philip Munsterman Tan, Inc. makes
Philip Munsterman Tan, Inc. manufactures the TAN Model I, a Class II medical device designed for [specific clinical purpose not detailed in data].
The TAN Model I is regulated under FDA’s Class II classification and requires a 510(k) clearance. The company is based in the United States.
Catalogue
Tan Model I Ref K853046
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Philip Munsterman Tan, Inc. have in the registry?
The registry currently lists 1 device for Philip Munsterman Tan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Philip Munsterman Tan, Inc.'s devices?
Among its 1 most recently registered device, Philip Munsterman Tan, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Philip Munsterman Tan, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Philip Munsterman Tan, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Philip Munsterman Tan, Inc. in the registry?
The most recently registered devices listed for Philip Munsterman Tan, Inc. include TAN MODEL I.