Medical Device Manufacturer · US , Anaheim , CA

Life Support Products, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1985
20
Total
20
Cleared
0
Denied

Life Support Products, Inc. has 20 FDA 510(k) cleared anesthesiology devices. Based in Anaheim, US.

Historical record: 20 cleared submissions from 1985 to 1995.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Life Support Products, Inc.
20 devices
1-12 of 20
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