Medical Device Manufacturer · US , Center Valley , PA

Aesculap - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2003

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap General Hospital ✕

3 devices

1-3 of 3

Cleared May 11, 2010

AESCULAP STERILCONTAINER S

General Hospital · 167d

Cleared Nov 17, 2006

AESCULAP STERILCONTAINER SYSTEM

General Hospital · 81d

Cleared Dec 06, 2004

AESCULAP STERRAD 100S COMPATABLE STERILCONTAINER

General Hospital · 248d