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. Obstetrics & Gynecology ✕
4 devices
Cleared
Jun 11, 2001
AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY
Obstetrics & Gynecology
90d
Cleared
Feb 20, 2001
SOVEREIGN BIPOLAR INSTRUMENTS FOR GYNECOLOGY
Obstetrics & Gynecology
90d
Cleared
Apr 25, 1995
AESCULAP LAPAROSCOPES
Obstetrics & Gynecology
320d
Cleared
Mar 29, 1995
AESCULAP LAPAROSCOPIC ANCILLARY DEVICES
Obstetrics & Gynecology
247d