Medcorp Intl.
Country not established
- Devices
- 1
What Medcorp Intl. makes
Medcorp Intl. manufactures the Flow I.V. Regulator Extension Set, a disposable intravenous administration device designed to control fluid flow rates in medical infusion systems.
The company’s products are regulated under FDA Class II devices and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Medcorp Flow I.V. Regulator Extension Set Ref K971004
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medcorp Intl. have in the registry?
The registry currently lists 1 device for Medcorp Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medcorp Intl.'s devices?
Among its 1 most recently registered device, Medcorp Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Medcorp Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medcorp Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medcorp Intl. in the registry?
The most recently registered devices listed for Medcorp Intl. include MEDCORP FLOW I.V. REGULATOR EXTENSION SET.