Repcocarts USA, Inc.
Country not established
- Devices
- 1
What Repcocarts USA, Inc. makes
Repcocarts USA, Inc. manufactures the REPCO Easy-Breather Clinical Air Pump, a device designed for delivering controlled airflow in clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with the REPCO Easy-Breather Clinical Air Pump listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Repco Easy-Breather Clinical Air Pump Ref K822512
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Repcocarts USA, Inc. have in the registry?
The registry currently lists 1 device for Repcocarts USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Repcocarts USA, Inc.'s devices?
Among its 1 most recently registered device, Repcocarts USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Repcocarts USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Repcocarts USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Repcocarts USA, Inc. in the registry?
The most recently registered devices listed for Repcocarts USA, Inc. include REPCO EASY-BREATHER CLINICAL AIR PUMP.