Knapps Corp.
Country not established
- Devices
- 1
What Knapps Corp. makes
Knapps Corp. manufactures THE BOOSTER, a medical device designed for [specific application—e.g., enhancing surgical outcomes, improving patient ventilation, or assisting in minimally invasive procedures—*not inferred; omit if unclear*].
THE BOOSTER is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
The Booster Ref K860698
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Knapps Corp. have in the registry?
The registry currently lists 1 device for Knapps Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Knapps Corp.'s devices?
Among its 1 most recently registered device, Knapps Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Knapps Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Knapps Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Knapps Corp. in the registry?
The most recently registered devices listed for Knapps Corp. include THE BOOSTER.