Larson Products, Inc.
Country not established
- Devices
- 1
What Larson Products, Inc. makes
Larson Products, Inc. manufactures the KLARITY, a medical device designed for diagnostic imaging or procedural guidance, though specific applications are not detailed.
The KLARITY 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
Klarity Ref K022708
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Larson Products, Inc. have in the registry?
The registry currently lists 1 device for Larson Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Larson Products, Inc.'s devices?
Among its 1 most recently registered device, Larson Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Larson Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Larson Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Larson Products, Inc. in the registry?
The most recently registered devices listed for Larson Products, Inc. include KLARITY.