Handren Assoc.
Country not established
- Devices
- 1
What Handren Assoc. makes
Handren Assoc. manufactures the QLICKSMART, a medical device designed for secure, rapid attachment and detachment of components in clinical or procedural settings, reducing manual handling and potential contamination.
The QLICKSMART is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Qlicksmart Ref K983367
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Handren Assoc. have in the registry?
The registry currently lists 1 device for Handren Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Handren Assoc.'s devices?
Among its 1 most recently registered device, Handren Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Handren Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Handren Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Handren Assoc. in the registry?
The most recently registered devices listed for Handren Assoc. include QLICKSMART.