Aesculap, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aesculap Aicon® Series Container System, XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set, SQ.line KERRISON
207
Total
201
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aesculap, Inc. Cardiovascular ✕
3 devices