Angiotech Pharmaceuticals, Inc.
Country not established
- Devices
- 1
What Angiotech Pharmaceuticals, Inc. makes
Angiotech Pharmaceuticals, Inc. manufactures central venous catheters (CVCs), including those designed for short- and long-term venous access in clinical settings.
The company’s products are regulated as Class II medical devices in the U.S. and are listed under the FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Angiotech Cvc Ref K073520
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiotech Pharmaceuticals, Inc. have in the registry?
The registry currently lists 1 device for Angiotech Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiotech Pharmaceuticals, Inc.'s devices?
Among its 1 most recently registered device, Angiotech Pharmaceuticals, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Angiotech Pharmaceuticals, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Angiotech Pharmaceuticals, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiotech Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Angiotech Pharmaceuticals, Inc. include ANGIOTECH CVC.