Mima-Pro Scientific, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Mima-Pro Scientific, Inc. makes
Mima-Pro Scientific, Inc. manufactures the SurBlate Ablation System, a device designed for precise tissue ablation procedures.
The SurBlate Ablate System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
SurBlate Ablation System Ref K223272
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mima-Pro Scientific, Inc. have in the registry?
The registry currently lists 1 device for Mima-Pro Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mima-Pro Scientific, Inc.'s devices?
Among its 1 most recently registered device, Mima-Pro Scientific, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mima-Pro Scientific, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mima-Pro Scientific, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mima-Pro Scientific, Inc. in the registry?
The most recently registered devices listed for Mima-Pro Scientific, Inc. include SurBlate Ablation System.