Lifestream Diagnostics, Inc.
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- Devices
- 1
What Lifestream Diagnostics, Inc. makes
Lifestream Diagnostics, Inc. manufactures the Cholestron PRO II, a cholesterol test designed for point-of-care or home use to measure total cholesterol levels in blood samples.
The Cholestron PRO II is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
Cholestron Pro Ii Cholesterol Test Ref K981345
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifestream Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Lifestream Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifestream Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Lifestream Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lifestream Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lifestream Diagnostics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lifestream Diagnostics, Inc. in the registry?
The most recently registered devices listed for Lifestream Diagnostics, Inc. include CHOLESTRON PRO II CHOLESTEROL TEST.