Freerider USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Freerider USA, Inc. makes
Freerider USA, Inc. manufactures Class II electrophysiological mapping catheters, including the FREERIDER models FR510-F and FR168-4, designed for cardiac electrophysiology procedures.
These devices are regulated under the FDA’s 510(k) pathway and are listed as Class II medical devices. The company is based in the United States.
Catalogue
Freerider, Model FR510-F Ref K971387
Regimes: 510(k) Registry: 510(k)Freerider, Model FR168-4 Ref K971388
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Freerider USA, Inc. have in the registry?
The registry currently lists 2 devices for Freerider USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Freerider USA, Inc.'s devices?
Among its 2 most recently registered devices, Freerider USA, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Freerider USA, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Freerider USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Freerider USA, Inc. in the registry?
The most recently registered devices listed for Freerider USA, Inc. include FREERIDER, MODEL FR510-F and FREERIDER, MODEL FR168-4.