Davol Inc., Sub. C. R. Bard, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Davol Inc., Sub. C. R. Bard, Inc. has 24 FDA 510(k) cleared medical devices. Based in Canston, US.
Historical record: 24 cleared submissions from 1994 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Davol Inc., Sub. C. R. Bard, Inc. Filter by specialty or product code using the sidebar.
24 devices
Cleared
Jul 15, 2010
VENTRALIGHT ST MESH
General & Plastic Surgery
14d
Cleared
Dec 08, 2009
BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150,...
General & Plastic Surgery
155d
Cleared
Oct 07, 2008
BARD 3DMAX MESH
General & Plastic Surgery
181d
Cleared
Oct 23, 2006
BARD COMPOSITE L/P MESH
General & Plastic Surgery
124d
Cleared
Jun 02, 2006
BARD EXTRA LARGE COMPOSIX KUGEL HERNIA PATCH
General & Plastic Surgery
22d
Cleared
Aug 11, 2005
SALUTE II DISPOSABLE FIXATION DEVICE, MODELS 0113070, 0113072, 0113073,...
General & Plastic Surgery
35d
Cleared
May 25, 2005
SALUTE FIXATION SYSTEM
General & Plastic Surgery
76d
Cleared
Aug 16, 2001
AQUASENS FLUID MONITORING SYSTEM
Obstetrics & Gynecology
129d
Cleared
Dec 08, 2000
NEZHAT-DORSEY REUSABLE ELECTROSURGICAL ATTACHMENTS: J-HOOK TIP, L-HOOK TIP,...
General & Plastic Surgery
9d
Cleared
Sep 13, 1999
DAVOL HYSTEROSCOPY POUCH DRAPE AND TUBING SET, MODEL OOXXXXO
Obstetrics & Gynecology
110d
Cleared
Jun 22, 1999
BARD SPERMA-TEX PRESHAPED MESH (2.4X5.6), MODEL 0114700
General & Plastic Surgery
41d
Cleared
Feb 19, 1999
HYDROFLEX HD HYSTEROSCOPIC DISTENTION SYSTEM,MODEL #'S 0025360, 0025370, 0025000
Obstetrics & Gynecology
189d