Medical Device Manufacturer · DE , Freiburg

Stockert GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Stockert GmbH Anesthesiology ✕

4 devices

1-4 of 4

Cleared Mar 22, 2007

MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098

Anesthesiology · 65d

Cleared Nov 21, 2006

Anesthesiology · 131d

Cleared Nov 17, 2005

STIMUPLEX HNS-12, MODEL 4892098

Anesthesiology · 84d

Cleared Jun 06, 2001

STIMUPLEX HNS-11

Anesthesiology · 162d