Hotspur Technologies, Inc Subsidiary of Teleflex ME
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- Devices
- 1
What Hotspur Technologies, Inc Subsidiary of Teleflex ME makes
Hotspur Technologies, Inc. manufactures the Arrow GPSCATH balloon dilatation catheter, a device designed for percutaneous coronary interventions to dilate narrowed or blocked coronary arteries.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The subsidiary is based in the United States.
Catalogue
Arrow Gpscath Balloon Dilatation Catheter Ref K140351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hotspur Technologies, Inc Subsidiary of Teleflex ME have in the registry?
The registry currently lists 1 device for Hotspur Technologies, Inc Subsidiary of Teleflex ME. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hotspur Technologies, Inc Subsidiary of Teleflex ME's devices?
Among its 1 most recently registered device, Hotspur Technologies, Inc Subsidiary of Teleflex ME has devices listed in FDA 510(k) (1 device).
What risk classes do Hotspur Technologies, Inc Subsidiary of Teleflex ME's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hotspur Technologies, Inc Subsidiary of Teleflex ME's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hotspur Technologies, Inc Subsidiary of Teleflex ME in the registry?
The most recently registered devices listed for Hotspur Technologies, Inc Subsidiary of Teleflex ME include ARROW GPSCATH BALLOON DILATATION CATHETER.