Lmt Lammers Medical Technology GmbH is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Lmt Lammers Medical Technology GmbH - FDA 510(k) Cleared Devices
Recent clearances: LMT NOMAG IC 3.0, LMT NOMAG IC 1,5
2
Total
2
Cleared
0
Denied
Lmt Lammers Medical Technology GmbH has 2 FDA 510(k) cleared medical devices. Based in Luebeck, DE.
Historical record: 2 cleared submissions from 2003 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Lmt Lammers Medical Technology GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Lmt Lammers Medical Technology GmbH
2 devices