Cook, Inc. - FDA 510(k) Cleared Devices
190
Total
179
Cleared
0
Denied
Cook, Inc. has 179 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 179 cleared submissions from 1976 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cook, Inc. Filter by specialty or product code using the sidebar.
190 devices
Cleared
Jan 09, 2015
BEACON TIP TORCON NB ADVANTAGE CATHETER, TORCON NB ADVANTAGE CATHETER
Cardiovascular
466d
Cleared
Dec 15, 2014
ADVANCE SALIVARY BALLOON CATHETER WITH WIRE GUIDE
General & Plastic Surgery
283d
Cleared
Oct 09, 2014
FLEXOR RADIAL HYDROPHILIC INTRODUCER ACCESS SET
Cardiovascular
416d
Cleared
Apr 18, 2014
CIAGLIA PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET/TRAY, CIAGLIA BLUE RHINO...
Anesthesiology
147d
Cleared
Feb 20, 2014
CANTATA(R) 2.9 MICROCATHETER
Cardiovascular
248d
Cleared
Jan 29, 2014
ADVANCE CS CORONARY SINUS INFUSION CATHETER
Cardiovascular
275d
Cleared
Dec 23, 2013
SPECTRUM TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET
General Hospital
27d
Cleared
Oct 25, 2013
ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETER
Cardiovascular
116d
Cleared
Oct 07, 2013
ENTUIT SECURE GASTROINTESTIONAL SUTURE ANCHOR SET, ENTUIT SECURE ADJUSTABLE...
Gastroenterology & Urology
161d
Cleared
Sep 27, 2013
COOK CERVICAL RIPENING BALLOON
Obstetrics & Gynecology
151d
Cleared
Aug 16, 2013
TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) SET
General Hospital
21d
Cleared
Jul 29, 2013
COOK TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY COOK SPECTRUM...
Gastroenterology & Urology
378d
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