Curtin & Associates International, Inc.
Country not established
- Devices
- 1
What Curtin & Associates International, Inc. makes
Curtin & Associates International, Inc. manufactures the RESPIFLO/S, a medical device designed for respiratory support or monitoring applications.
The RESPIFLO/S is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Respiflo/S Ref K962874
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Curtin & Associates International, Inc. have in the registry?
The registry currently lists 1 device for Curtin & Associates International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curtin & Associates International, Inc.'s devices?
Among its 1 most recently registered device, Curtin & Associates International, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Curtin & Associates International, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Curtin & Associates International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curtin & Associates International, Inc. in the registry?
The most recently registered devices listed for Curtin & Associates International, Inc. include RESPIFLO/S.