K&S Assoc., Inc.
Country not established
- Devices
- 1
What K&S Assoc., Inc. makes
K&S Assoc., Inc. makes medical devices such as the DIAMOND SETUP 2000.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Diamond Setup 2000 Ref K032886
510(k) 510(k)
Frequently asked questions
How many devices does K&S Assoc., Inc. have in the registry?
The registry currently lists 1 device for K&S Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K&S Assoc., Inc.'s devices?
Among its 1 most recently registered device, K&S Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do K&S Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for K&S Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from K&S Assoc., Inc. in the registry?
The most recently registered devices listed for K&S Assoc., Inc. include DIAMOND SETUP 2000.