Medical Device Manufacturer · US , Dover , DE

Quality Life Technologies Co;Ltd - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012
1
Total
1
Cleared
0
Denied

Quality Life Technologies Co;Ltd has 1 FDA 510(k) cleared medical devices. Based in Dover, US.

Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Quality Life Technologies Co;Ltd Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Quality Life Technologies Co;Ltd
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