Carrtech Corp
Country not established
- Devices
- 1
What Carrtech Corp makes
Carrtech Corp manufactures the FROG (Filter Removal of Glass), a device designed to remove glass particles from intravenous lines and medical tubing to prevent contamination and potential patient injury.
The FROG device is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. Carrtech Corp is based in the United States.
Catalogue
FROG (Filter Removal of Glass) Ref K240355
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Carrtech Corp have in the registry?
The registry currently lists 1 device for Carrtech Corp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carrtech Corp's devices?
Among its 1 most recently registered device, Carrtech Corp has devices listed in FDA 510(k) (1 device).
What risk classes do Carrtech Corp's devices fall under?
Among its 1 most recently registered device, the classes recorded for Carrtech Corp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carrtech Corp in the registry?
The most recently registered devices listed for Carrtech Corp include FROG (Filter Removal of Glass).