FDA 510(k) Applications Submitted by DAVOL INC., SUB. C.R. BARD, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K061754 |
06/21/2006 |
BARD COMPOSITE L/P MESH |
DAVOL INC., SUB. C.R. BARD, INC. |
| K092032 |
07/06/2009 |
BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160 |
DAVOL INC., SUB. C.R. BARD, INC. |
| K050610 |
03/10/2005 |
SALUTE FIXATION SYSTEM |
DAVOL INC., SUB. C.R. BARD, INC. |
| K051848 |
07/07/2005 |
SALUTE II DISPOSABLE FIXATION DEVICE, MODELS 0113070, 0113072, 0113073, 0113077, 0113079 |
DAVOL INC., SUB. C.R. BARD, INC. |
| K101851 |
07/01/2010 |
VENTRALIGHT ST MESH |
DAVOL INC., SUB. C.R. BARD, INC. |
| K061314 |
05/11/2006 |
BARD EXTRA LARGE COMPOSIX KUGEL HERNIA PATCH |
DAVOL INC., SUB. C.R. BARD, INC. |
| K081010 |
04/09/2008 |
BARD 3DMAX MESH |
DAVOL INC., SUB. C.R. BARD, INC. |
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