Kelsey, Inc.
Country not established
- Devices
- 1
What Kelsey, Inc. makes
Kelsey, Inc. manufactures the Kelsey Intersitial Laser Therapy System, a device designed for interstitial laser ablation used in medical procedures.
The company’s portfolio is regulated under Class II devices in the US, with the Kelsey Intersitial Laser Therapy System listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Kelsey Intersitital Laser Therapy System Ref K070353
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kelsey, Inc. have in the registry?
The registry currently lists 1 device for Kelsey, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kelsey, Inc.'s devices?
Among its 1 most recently registered device, Kelsey, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kelsey, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kelsey, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kelsey, Inc. in the registry?
The most recently registered devices listed for Kelsey, Inc. include KELSEY INTERSITITAL LASER THERAPY SYSTEM.