Micardia Corporation
Country not established
- Devices
- 1
What Micardia Corporation makes
Micardia Corporation produces the MICARDIA ANNULOPLASTY BAND DR, a medical device used for annuloplasty procedures.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Micardia Annuloplasty Band Dr Ref K070488
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micardia Corporation have in the registry?
The registry currently lists 1 device for Micardia Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micardia Corporation's devices?
Among its 1 most recently registered device, Micardia Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Micardia Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Micardia Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micardia Corporation in the registry?
The most recently registered devices listed for Micardia Corporation include MICARDIA ANNULOPLASTY BAND DR.