Lauer Ltd., Hong Kong is one of 472 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Lauer Ltd., Hong Kong - FDA 510(k) Cleared Devices
Recent clearances: AQUABOSS ECORO DIA 50
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.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Lauer Ltd., Hong Kong
1 devices