Kahn-Tact U.S.A., Inc.
Country not established
- Devices
- 1
What Kahn-Tact U.S.A., Inc. makes
Kahn-Tact U.S.A., Inc. manufactures the SOLCO Silicone Resuscitator, a device designed for manual ventilation during resuscitation procedures.
The SOLCO Silicone Resuscitator is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Solco Silicone Resuscitator Ref K874321
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kahn-Tact U.S.A., Inc. have in the registry?
The registry currently lists 1 device for Kahn-Tact U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kahn-Tact U.S.A., Inc.'s devices?
Among its 1 most recently registered device, Kahn-Tact U.S.A., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kahn-Tact U.S.A., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kahn-Tact U.S.A., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kahn-Tact U.S.A., Inc. in the registry?
The most recently registered devices listed for Kahn-Tact U.S.A., Inc. include SOLCO SILICONE RESUSCITATOR.