Thermopeutix, Inc. Dba Ymed, Inc.
Country not established
- Devices
- 1
What Thermopeutix, Inc. Dba Ymed, Inc. makes
Thermopeutix, Inc. (dba Ymed, Inc.) manufactures the VASCUTRAK II, a percutaneous transluminal angioplasty (PTA) dilatation catheter designed for vascular interventions to treat peripheral artery disease.
The company’s portfolio is regulated under FDA Class II devices, with the VASCUTRAK II listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Vascutrak Ii Pta Dilatation Catheter Ref K073025
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thermopeutix, Inc. Dba Ymed, Inc. have in the registry?
The registry currently lists 1 device for Thermopeutix, Inc. Dba Ymed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thermopeutix, Inc. Dba Ymed, Inc.'s devices?
Among its 1 most recently registered device, Thermopeutix, Inc. Dba Ymed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Thermopeutix, Inc. Dba Ymed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Thermopeutix, Inc. Dba Ymed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thermopeutix, Inc. Dba Ymed, Inc. in the registry?
The most recently registered devices listed for Thermopeutix, Inc. Dba Ymed, Inc. include VASCUTRAK II PTA DILATATION CATHETER.