Kdk Corp.
JapanFDA applicant, unverified
- Devices
- 1
What Kdk Corp. makes
Kdk Corp. manufactures the Lactate Pro System, a device designed for measuring blood lactate levels to assess metabolic performance and exercise intensity.
The Lactate Pro System is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Lactate Pro System Ref K980908
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kdk Corp. have in the registry?
The registry currently lists 1 device for Kdk Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kdk Corp.'s devices?
Among its 1 most recently registered device, Kdk Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Kdk Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kdk Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kdk Corp. in the registry?
The most recently registered devices listed for Kdk Corp. include LACTATE PRO SYSTEM.