Kohler Medizintechnik GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: PERMAFIX CHAIRSIDE SOFT DENTURE RELINING (7010) (7011-13) (7014-15)
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kohler Medizintechnik GmbH & Co. KG Dental ✕
1 devices