Mitsubishi Cable America, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Mitsubishi Cable America, Inc. makes
Mitsubishi Cable America, Inc. manufactures endoscopic equipment, including endoscope introducer kits, ultrathin flexible endoscopes (such as the TAS-211/2.3), and battery-powered endoscopic light sources for medical imaging procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Endoscope Introducer Kit Ref K955717
Regimes: 510(k) Registry: 510(k)Ultrathin Flexible Endoscope Tas-211/2.3 Ref K936257
Regimes: 510(k) Registry: 510(k)Battery Powered Endosccopic Light Source Ref K960081
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mitsubishi Cable America, Inc. have in the registry?
The registry currently lists 3 devices for Mitsubishi Cable America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mitsubishi Cable America, Inc.'s devices?
Among its 3 most recently registered devices, Mitsubishi Cable America, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mitsubishi Cable America, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mitsubishi Cable America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mitsubishi Cable America, Inc. in the registry?
The most recently registered devices listed for Mitsubishi Cable America, Inc. include ENDOSCOPE INTRODUCER KIT, ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3 and BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE.