Lifestream Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
- Regimes: 510(k) Registry: 510(k)
Resolution Cholesterol Monitor Ref K000610
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifestream Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Lifestream Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifestream Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Lifestream Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Lifestream Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lifestream Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lifestream Technologies, Inc. in the registry?
The most recently registered devices listed for Lifestream Technologies, Inc. include LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR, RESOLUTION CHOLESTEROL MONITOR and PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR.