FDA 510(k) Applications Submitted by DYNAREX CORP.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K052314 |
08/25/2005 |
DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE |
DYNAREX CORP. |
| K052743 |
09/30/2005 |
DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921 |
DYNAREX CORP. |
| K012816 |
08/22/2001 |
DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414 |
DYNAREX CORP. |
| K012917 |
08/30/2001 |
DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B |
DYNAREX CORP. |
| K012957 |
09/04/2001 |
TOWEL DRAPE, MODELS 4409, 4410 |
DYNAREX CORP. |
| K960388 |
01/26/1996 |
DYNAREX NON-WOVEN SPONGE |
DYNAREX CORP. |
| K991694 |
05/18/1999 |
DYNAREX DRAIN SPONGE |
DYNAREX CORP. |
| K991695 |
05/18/1999 |
DYNAREX NON-WOVEN SPONGE |
DYNAREX CORP. |
| K983348 |
09/23/1998 |
DYNAREX TRACHEOSTOMY SPONGE |
DYNAREX CORP. |
|
|
