Bennett and Assoc., Inc.
Country not established
- Devices
- 1
What Bennett and Assoc., Inc. makes
Bennett and Assoc., Inc. manufactures the SPECTRADOP, a medical device designed for respiratory monitoring and support, specifically for measuring and analyzing respiratory waveforms and parameters.
The SPECTRADOP is classified as a Class II device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
Spectradop Ref K925078
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bennett and Assoc., Inc. have in the registry?
The registry currently lists 1 device for Bennett and Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bennett and Assoc., Inc.'s devices?
Among its 1 most recently registered device, Bennett and Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bennett and Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bennett and Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bennett and Assoc., Inc. in the registry?
The most recently registered devices listed for Bennett and Assoc., Inc. include SPECTRADOP.