Peter Martin Associates, Inc.
Country not established
- Devices
- 1
What Peter Martin Associates, Inc. makes
Peter Martin Associates, Inc. manufactures the SVENSK TK/2, a medical device designed for tracheostomy care, including tracheostomy tubes and related accessories.
The SVENSK TK/2 is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Svensk Tk/2 Ref K820503
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peter Martin Associates, Inc. have in the registry?
The registry currently lists 1 device for Peter Martin Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peter Martin Associates, Inc.'s devices?
Among its 1 most recently registered device, Peter Martin Associates, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Peter Martin Associates, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Peter Martin Associates, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Peter Martin Associates, Inc. in the registry?
The most recently registered devices listed for Peter Martin Associates, Inc. include SVENSK TK/2.