Bomed, Inc.
Country not established
- Devices
- 1
What Bomed, Inc. makes
Bomed, Inc. manufactures the TEBCO-W, a device designed for transesophageal cardiac output monitoring, which measures blood flow through the heart via a catheter inserted through the esophagus.
The TEBCO-W is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Tebco-W Ref K132892
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bomed, Inc. have in the registry?
The registry currently lists 1 device for Bomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bomed, Inc.'s devices?
Among its 1 most recently registered device, Bomed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bomed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bomed, Inc. in the registry?
The most recently registered devices listed for Bomed, Inc. include TEBCO-W.