Mc3 Incorporated
United StatesFDA applicant, unverified
- Devices
- 4
What Mc3 Incorporated makes
Mc3 Incorporated manufactures medical devices including the Nautilus Smart ECMO Module, MC3 Jugular Dual Lumen Catheter, MC3 QuickFlow Dual Lumen Catheter, and MC3 Vascular Access Kit 21030.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Mc3 Incorporated is based in the US.
Catalogue
Nautilus Smart ECMO Module Ref K191935
Regimes: 510(k) Registry: 510(k)MC3 Jugular Dual Lumen Catheter Ref K180151
Regimes: 510(k) Registry: 510(k)MC3 QuickFlow Dual Lumen Catheter Ref K171610
Regimes: 510(k) Registry: 510(k)MC3 Vascular Access Kit 21030 Ref K182914
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mc3 Incorporated have in the registry?
The registry currently lists 4 devices for Mc3 Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mc3 Incorporated's devices?
Among its 4 most recently registered devices, Mc3 Incorporated has devices listed in FDA 510(k) (4 devices).
What risk classes do Mc3 Incorporated's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mc3 Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mc3 Incorporated in the registry?
The most recently registered devices listed for Mc3 Incorporated include Nautilus Smart ECMO Module, MC3 Jugular Dual Lumen Catheter, MC3 QuickFlow Dual Lumen Catheter and MC3 Vascular Access Kit 21030.