Medical Device Manufacturer · US , Sugar Land , TX

Lifestream Int'L, Inc. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1984
23
Total
23
Cleared
0
Denied

Lifestream Int'L, Inc. has 23 FDA 510(k) cleared medical devices. Based in Sugar Land, US.

Historical record: 23 cleared submissions from 1984 to 1997.

Browse the FDA 510(k) cleared devices submitted by Lifestream Int'L, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Lifestream Int'L, Inc.

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