Micro Interventional Systems, Inc.
Country not established
- Devices
- 1
What Micro Interventional Systems, Inc. makes
Micro Interventional Systems, Inc. makes the OmniGuide guiding catheter with balloon, a device used to guide and support other instruments during vascular procedures while providing temporary occlusion via an inflatable balloon.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
The Omniguide Guiding Catheter With Balloon Ref K945963
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micro Interventional Systems, Inc. have in the registry?
The registry currently lists 1 device for Micro Interventional Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micro Interventional Systems, Inc.'s devices?
Among its 1 most recently registered device, Micro Interventional Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Micro Interventional Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Micro Interventional Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micro Interventional Systems, Inc. in the registry?
The most recently registered devices listed for Micro Interventional Systems, Inc. include THE OMNIGUIDE GUIDING CATHETER WITH BALLOON.