Medical Device Manufacturer · US , Center Valley , PA

Aesculap, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared May 04, 2012

STERILCONTAINER SYSTEM

General Hospital · 233d