John Caunt Scientific, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What John Caunt Scientific, Ltd. makes
John Caunt Scientific, Ltd. manufactures the SOURCERER, a medical device designed for [specific function not provided in data]. This product falls under Class I devices, indicating it poses minimal risk and is typically exempt from stringent pre-market review requirements.
The SOURCERER is listed in the FDA’s 510(k) registry, demonstrating compliance with U.S. regulatory requirements for Class I devices. The company is based in the United States.
Catalogue
Sourcerer Ref K884091
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does John Caunt Scientific, Ltd. have in the registry?
The registry currently lists 1 device for John Caunt Scientific, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list John Caunt Scientific, Ltd.'s devices?
Among its 1 most recently registered device, John Caunt Scientific, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do John Caunt Scientific, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for John Caunt Scientific, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from John Caunt Scientific, Ltd. in the registry?
The most recently registered devices listed for John Caunt Scientific, Ltd. include SOURCERER.