Medical Device Manufacturer · US , Newport Beach , CA

Kerr Corporation - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 2006

32

Total

32

Cleared

0

Denied

32 devices

26-32 of 32

Cleared Jan 27, 2010

PREMISE FLOWABLE MODIFIED

Cleared May 21, 2009

Cleared Jan 29, 2008

Cleared Sep 10, 2007

TI2200 TRANSILLUMINATION CABLE

Cleared Jul 26, 2007

Cleared Oct 19, 2006

Cleared Apr 28, 2006

PREMISE FLOWABLE