Qrc Consulting
Country not established
- Devices
- 1
What Qrc Consulting makes
Qrc Consulting manufactures the SUTURTEK FASTCLOSE FASCIA CLOSURE DEVICE, a Class II medical device used for fascia closure procedures.
The company is based in the US and its device is listed in the FDA 510(k) registry, indicating it is a Class II device cleared for market entry.
Catalogue
Suturtek Fastclose Fascia Closure Device Ref K011105
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Qrc Consulting have in the registry?
The registry currently lists 1 device for Qrc Consulting. Devices recorded under merged duplicate company entries are counted once.
Which registries list Qrc Consulting's devices?
Among its 1 most recently registered device, Qrc Consulting has devices listed in FDA 510(k) (1 device).
What risk classes do Qrc Consulting's devices fall under?
Among its 1 most recently registered device, the classes recorded for Qrc Consulting's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Qrc Consulting in the registry?
The most recently registered devices listed for Qrc Consulting include SUTURTEK FASTCLOSE FASCIA CLOSURE DEVICE.