Accuro Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Accuro Technologies, Inc. makes
Accuro Technologies, Inc. manufactures the ARTHROTAP, a device used for orthopedic procedures to assist in joint aspiration or injection, such as knee arthrocentesis.
The ARTHROTAP is classified as a Class II medical device in the U.S. and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
Arthrotap Ref K201816
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accuro Technologies, Inc. have in the registry?
The registry currently lists 1 device for Accuro Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accuro Technologies, Inc.'s devices?
Among its 1 most recently registered device, Accuro Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Accuro Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Accuro Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accuro Technologies, Inc. in the registry?
The most recently registered devices listed for Accuro Technologies, Inc. include ARTHROTAP.