Dispos-A-Scope
Country not established
- Devices
- 1
What Dispos-A-Scope makes
Dispos-A-Scope manufactures the DISPOS-A-SCOPE, a single-use endoscopic device designed for diagnostic and therapeutic procedures.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Dispos-A-Scope Ref K993738
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dispos-A-Scope have in the registry?
The registry currently lists 1 device for Dispos-A-Scope. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dispos-A-Scope's devices?
Among its 1 most recently registered device, Dispos-A-Scope has devices listed in FDA 510(k) (1 device).
What risk classes do Dispos-A-Scope's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dispos-A-Scope's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dispos-A-Scope in the registry?
The most recently registered devices listed for Dispos-A-Scope include DISPOS-A-SCOPE.