Kps & Assoc., Inc.
Country not established
- Devices
- 1
What Kps & Assoc., Inc. makes
Kps & Assoc., Inc. manufactures the TRAPIS (Transperineal Prostate Implant Simulator), version 1.5, a medical device used for prostate implant procedures.
The TRAPIS device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Kps & Assoc., Inc. have in the registry?
The registry currently lists 1 device for Kps & Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kps & Assoc., Inc.'s devices?
Among its 1 most recently registered device, Kps & Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kps & Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kps & Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kps & Assoc., Inc. in the registry?
The most recently registered devices listed for Kps & Assoc., Inc. include TRAPIS (TRANSPERINEAL PROSTATE IMPLANT SIMULATOR), VERSION 1.5.