Flaitron Laboratories, Inc.
Country not established
- Devices
- 1
What Flaitron Laboratories, Inc. makes
Flaitron Laboratories, Inc. manufactures NEPHROLYTE, a medical device designed for intravenous administration to manage electrolyte imbalances in patients.
The device is classified under Class I by the FDA and is listed in the 510(k) registry. The company is based in the United States.
Catalogue
Nephrolyte Ref K831502
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flaitron Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Flaitron Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flaitron Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Flaitron Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Flaitron Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Flaitron Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Flaitron Laboratories, Inc. in the registry?
The most recently registered devices listed for Flaitron Laboratories, Inc. include NEPHROLYTE.