Kaybath, Inc.
Country not established
- Devices
- 1
What Kaybath, Inc. makes
Kaybath, Inc. manufactures the NATURALYTE (Model # 08-4004-1), a medical device designed for electrolyte replenishment in patients requiring intravenous hydration.
The NATURALYTE falls under FDA Class II regulation and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
Naturalyte, Model # 08-4004-1 Ref K982813
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kaybath, Inc. have in the registry?
The registry currently lists 1 device for Kaybath, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kaybath, Inc.'s devices?
Among its 1 most recently registered device, Kaybath, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kaybath, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kaybath, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kaybath, Inc. in the registry?
The most recently registered devices listed for Kaybath, Inc. include NATURALYTE, MODEL # 08-4004-1.