Lifestream Technologies, Inc. is one of 23893 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lifestream Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIFESTREAM PLUS CHOLESTEROL MONITOR, MODIFICATION TO RESOLUTION CHOLESTEROL MONITOR, RESOLUTION CHOLESTEROL MONITOR, PRIVALINK SOFTWARE ACCESSORY TO THE LIFESTREAM CHOLESTEROL MONITOR
3
Total
3
Cleared
0
Denied
Lifestream Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Post Falls, US.
Historical record: 3 cleared submissions from 1999 to 2004. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Lifestream Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lifestream Technologies, Inc.
3 devices