Strenumed, Inc.
Country not established
- Devices
- 1
What Strenumed, Inc. makes
Strenumed, Inc. manufactures replacement batteries for the SYSTEM 2000 and SYSTEM 2000-EXTENDED RUN medical devices, designed to extend operational runtime.
These products fall under FDA Class I regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Strenumed, Inc. have in the registry?
The registry currently lists 1 device for Strenumed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Strenumed, Inc.'s devices?
Among its 1 most recently registered device, Strenumed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Strenumed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Strenumed, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Strenumed, Inc. in the registry?
The most recently registered devices listed for Strenumed, Inc. include SYSTEM 2000 REPLACEMENT BATTERY, SYSTEM 2000-EXTENDED RUN REPLACEMENT BATTERY.