Medtronic Versaflex, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medtronic Versaflex, Inc. makes
Medtronic Versaflex, Inc. manufactures percutaneous transangioplasty catheters (models 6526, 6527, 6528) and a contrast injection device (model 611101) for angiographic procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Model 611101 Contrast Injection Device Ref K890898
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Versaflex, Inc. have in the registry?
The registry currently lists 2 devices for Medtronic Versaflex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Versaflex, Inc.'s devices?
Among its 2 most recently registered devices, Medtronic Versaflex, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medtronic Versaflex, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medtronic Versaflex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Versaflex, Inc. in the registry?
The most recently registered devices listed for Medtronic Versaflex, Inc. include MODELS 6526, 6527, 6528 PERCU. TRANS. ANGIO. CATH. and MODEL 611101 CONTRAST INJECTION DEVICE.