Cryo Vascular Systems, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
Catalogue
Polar Cath Peripheral Dilatation System Ref K051916
510(k) 510(k)- 510(k) 510(k)
Polarcath Peripheral Dilatation System Ref K033622
510(k) 510(k)Polarcath Peripheral Balloon Catheter System Ref K030742
510(k) 510(k)- 510(k) 510(k)
Cvsi Peripheral Balloon Catheter; Cvsi Inflater Ref K022061
510(k) 510(k)Polarcath Peripheral Balloon Catheter System Ref K042230
510(k) 510(k)
Frequently asked questions
How many devices does Cryo Vascular Systems, Inc. have in the registry?
The registry currently lists 7 devices for Cryo Vascular Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryo Vascular Systems, Inc.'s devices?
Among its 7 most recently registered devices, Cryo Vascular Systems, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Cryo Vascular Systems, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Cryo Vascular Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryo Vascular Systems, Inc. in the registry?
The most recently registered devices listed for Cryo Vascular Systems, Inc. include POLAR CATH PERIPHERAL DILATATION SYSTEM, CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT, POLARCATH PERIPHERAL DILATATION SYSTEM and POLARCATH PERIPHERAL BALLOON CATHETER SYSTEM.