Mizzy, Inc.
Country not established
- Devices
- 1
What Mizzy, Inc. makes
Mizzy, Inc. manufactures the Mizzy Syrijet Mark IV, a medical device used for specific clinical applications as indicated by its classification.
The Mizzy Syrijet Mark IV is a Class II device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Mizzy Syrijet Mark Iv Ref K790193
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mizzy, Inc. have in the registry?
The registry currently lists 1 device for Mizzy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mizzy, Inc.'s devices?
Among its 1 most recently registered device, Mizzy, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mizzy, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mizzy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mizzy, Inc. in the registry?
The most recently registered devices listed for Mizzy, Inc. include MIZZY SYRIJET MARK IV.