Blakbag, Ltd., Division of Coherent Systems
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- Devices
- 1
What Blakbag, Ltd., Division of Coherent Systems makes
Blakbag, Ltd., Division of Coherent Systems makes the E-FAX SYSTEM.
The E-FAX SYSTEM is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
E-Fax System Ref K982034
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Blakbag, Ltd., Division of Coherent Systems have in the registry?
The registry currently lists 1 device for Blakbag, Ltd., Division of Coherent Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blakbag, Ltd., Division of Coherent Systems's devices?
Among its 1 most recently registered device, Blakbag, Ltd., Division of Coherent Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Blakbag, Ltd., Division of Coherent Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Blakbag, Ltd., Division of Coherent Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Blakbag, Ltd., Division of Coherent Systems in the registry?
The most recently registered devices listed for Blakbag, Ltd., Division of Coherent Systems include E-FAX SYSTEM.