Mayfield Instruments, Ltd.
CanadaFDA applicant, unverified
- Devices
- 1
What Mayfield Instruments, Ltd. makes
Mayfield Instruments, Ltd. manufactures the KEYFILL, a medical device designed for filling or injecting substances into medical devices or procedures.
The KEYFILL 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
Keyfill Ref K872053
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mayfield Instruments, Ltd. have in the registry?
The registry currently lists 1 device for Mayfield Instruments, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mayfield Instruments, Ltd.'s devices?
Among its 1 most recently registered device, Mayfield Instruments, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mayfield Instruments, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mayfield Instruments, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mayfield Instruments, Ltd. in the registry?
The most recently registered devices listed for Mayfield Instruments, Ltd. include KEYFILL.