Minnesota Medical Development, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Minnesota Medical Development, Inc. makes
Minnesota Medical Development, Inc. manufactures heart rate devices classified under the Rebound category, including the Rebound HRD, Rebound HRDV, and modifications to the Rebound HRD. These devices are designed for monitoring and recording heart rate data, likely intended for clinical or patient use.
The company’s portfolio consists of Class II medical devices, which are regulated under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Modification To Rebound Hrd Ref K080393
Regimes: 510(k) Registry: 510(k)Rebound Hrd Ref K063671
Regimes: 510(k) Registry: 510(k)Rebound Hrdv Ref K083467
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Minnesota Medical Development, Inc. have in the registry?
The registry currently lists 3 devices for Minnesota Medical Development, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minnesota Medical Development, Inc.'s devices?
Among its 3 most recently registered devices, Minnesota Medical Development, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Minnesota Medical Development, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Minnesota Medical Development, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Minnesota Medical Development, Inc. in the registry?
The most recently registered devices listed for Minnesota Medical Development, Inc. include MODIFICATION TO REBOUND HRD, REBOUND HRD and REBOUND HRDV.