Micro-Rel
Country not established
- Devices
- 1
What Micro-Rel makes
Micro-Rel manufactures the Pulstron Model 100, a Class III implantable device designed for cardiac pacing or resynchronization therapy.
The Pulstron Model 100 is regulated under the FDA’s 510(k) pathway as a Class III device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Pulstron Model 100 Ref K781835
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micro-Rel have in the registry?
The registry currently lists 1 device for Micro-Rel. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micro-Rel's devices?
Among its 1 most recently registered device, Micro-Rel has devices listed in FDA 510(k) (1 device).
What risk classes do Micro-Rel's devices fall under?
Among its 1 most recently registered device, the classes recorded for Micro-Rel's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Micro-Rel in the registry?
The most recently registered devices listed for Micro-Rel include PULSTRON MODEL 100.