Mainsfield Scientific, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
What Mainsfield Scientific, Inc. makes
Mainsfield Scientific, Inc. manufactures the NAVIGATOR, which is a medical device.
The company is based in the US, and its portfolio includes Class III devices that are listed in the FDA 510(k) registry.
Catalogue
Endomyocardial Biopsy Device Ref K870186
Regimes: 510(k) Registry: 510(k)Ciribart Gyudubg Catgeter Ref K855103
Regimes: 510(k) Registry: 510(k)Explorer Ref K853850
Regimes: 510(k) Registry: 510(k)Wedge Pressure Catheter Flow Directed Ref K841705
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Heparin Coat Tran Ballo Tip Temp Pac Electrode Ref K852797
Regimes: 510(k) Registry: 510(k)Angioscope Ref K865017
Regimes: 510(k) Registry: 510(k)Navigator Ref K853747
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mainsfield Scientific, Inc. have in the registry?
The registry currently lists 9 devices for Mainsfield Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mainsfield Scientific, Inc.'s devices?
Among its 9 most recently registered devices, Mainsfield Scientific, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Mainsfield Scientific, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Mainsfield Scientific, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Mainsfield Scientific, Inc. in the registry?
The most recently registered devices listed for Mainsfield Scientific, Inc. include ENDOMYOCARDIAL BIOPSY DEVICE, CIRIBART GYUDUBG CATGETER, EXPLORER and WEDGE PRESSURE CATHETER FLOW DIRECTED.