Med ET AL Development
United Statesfrom the FDA registration address FDA FEI 1000305409
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Med ET AL Development makes
Med ET AL Development manufactures the T-GUARD, a medical device designed for protective or monitoring applications in clinical settings, such as shielding or isolation purposes during procedures.
The T-GUARD is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
T-Guard Ref K945537
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000305409
- Address
- 1226 Mann Dr Ste 200, MATTHEWS, NC, 28105
Frequently asked questions
How many devices does Med ET AL Development have in the registry?
The registry currently lists 1 device for Med ET AL Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med ET AL Development's devices?
Among its 1 most recently registered device, Med ET AL Development has devices listed in FDA 510(k) (1 device).
What risk classes do Med ET AL Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Med ET AL Development's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Med ET AL Development in the registry?
The most recently registered devices listed for Med ET AL Development include T-GUARD.