Cook Biotech Incorprated is one of 4884 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cook Biotech Incorprated - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cook Biotech Incorprated has 4 FDA 510(k) cleared medical devices. Based in West Lafayette, US.
Historical record: 4 cleared submissions from 2013 to 2015. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Cook Biotech Incorprated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cook Biotech Incorprated
4 devices
Cleared
Dec 09, 2015
Biodesign Enterocutaneous Fistula Plug
General & Plastic Surgery
268d
Cleared
Oct 01, 2015
SIS Inguinal Hernia Repair Graft
General & Plastic Surgery
364d
Cleared
Sep 16, 2015
Biodesign Otologic Repair Graft
Ear, Nose, Throat
191d
Cleared
Feb 27, 2013
BIODESIGN ENT REPAIR GRAFT
Ear, Nose, Throat
296d