Nesa Medtech Private Limited
IndiaFDA applicant, unverified
- Devices
- 1
What Nesa Medtech Private Limited makes
Nesa Medtech Private Limited develops the Fibroid Mapping Reviewer Application (FMRA), a software tool designed for reviewing and analyzing fibroid mapping data in medical imaging.
The FMRA is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Fibroid Mapping Reviewer Application (FMRA) Ref K222683
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nesa Medtech Private Limited have in the registry?
The registry currently lists 1 device for Nesa Medtech Private Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nesa Medtech Private Limited's devices?
Among its 1 most recently registered device, Nesa Medtech Private Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Nesa Medtech Private Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nesa Medtech Private Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nesa Medtech Private Limited in the registry?
The most recently registered devices listed for Nesa Medtech Private Limited include Fibroid Mapping Reviewer Application (FMRA).