T-Med, Inc.
Country not established
- Devices
- 1
What T-Med, Inc. makes
T-Med, Inc. manufactures the Booty Endoscope Warmer, a device designed to maintain the temperature of endoscopes during cleaning and storage to ensure patient safety and device integrity.
The Booty Endoscope Warmer is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Booty Endoscope Warmer Ref K933515
510(k) 510(k)
Frequently asked questions
How many devices does T-Med, Inc. have in the registry?
The registry currently lists 1 device for T-Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list T-Med, Inc.'s devices?
Among its 1 most recently registered device, T-Med, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do T-Med, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for T-Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from T-Med, Inc. in the registry?
The most recently registered devices listed for T-Med, Inc. include BOOTY ENDOSCOPE WARMER.