Chest Innovations, Inc.
Country not established
- Devices
- 1
What Chest Innovations, Inc. makes
Chest Innovations, Inc. manufactures the SURECORE BIOPSY DEVICE, a Class II medical device designed for biopsy procedures.
This device is regulated under the FDA 510(k) pathway and is listed in the fda_510k registry. The company is based in the US.
Catalogue
Surecore Biopsy Device Ref K102756
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chest Innovations, Inc. have in the registry?
The registry currently lists 1 device for Chest Innovations, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chest Innovations, Inc.'s devices?
Among its 1 most recently registered device, Chest Innovations, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Chest Innovations, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Chest Innovations, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chest Innovations, Inc. in the registry?
The most recently registered devices listed for Chest Innovations, Inc. include SURECORE BIOPSY DEVICE.