Vascucare, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Vascucare, Inc. makes
Vascucare, Inc. manufactures medical devices for vascular and respiratory applications, including a real-time monitoring system for respiratory airway tubes, a percutaneous angioscopy delivery system for vascular procedures, and an angiopump for controlled fluid management in angiographic settings.
The company’s portfolio consists of Class II devices, all of which are authorised via the FDA’s 510(k) clearance process. These devices are listed under the US regulatory framework and are intended for commercial distribution within the United States.
Catalogue
Respiratory Airway Tube Monitor (Ratm) Ref K883158
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Vascu-Care Angioscope Ref K880927
Regimes: 510(k) Registry: 510(k)Vascucare Angiopump Ref K881780
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascucare, Inc. have in the registry?
The registry currently lists 4 devices for Vascucare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascucare, Inc.'s devices?
Among its 4 most recently registered devices, Vascucare, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Vascucare, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Vascucare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vascucare, Inc. in the registry?
The most recently registered devices listed for Vascucare, Inc. include RESPIRATORY AIRWAY TUBE MONITOR (RATM), VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM, VASCU-CARE ANGIOSCOPE and VASCUCARE ANGIOPUMP.