Medical Device Manufacturer · DE , Wittlingen

Lauer Ltd., Hong Kong - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003
1
Total
1
Cleared
0
Denied

Lauer Ltd., Hong Kong has 1 FDA 510(k) cleared medical devices. Based in Wittlingen, DE.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Lauer Ltd., Hong Kong Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lauer Ltd., Hong Kong

1 devices
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