FDA 510(k) Applications Submitted by PROMEX, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960023 |
01/02/1996 |
KIRSHNER WIRES (K-WIRE) & STEINMANN PINS |
PROMEX, INC. |
| K960405 |
01/29/1996 |
SPINAL NEEDLE |
PROMEX, INC. |
| K010400 |
02/12/2001 |
VACUUM ASSISTED CORE BIOPSY DEVICE |
PROMEX, INC. |
| K001132 |
04/10/2000 |
BONE BIOPSY NEEDLE |
PROMEX, INC. |
| K011270 |
04/26/2001 |
AUTOMATED CORE BIOPSY DEVICE |
PROMEX, INC. |
| K972865 |
08/04/1997 |
PROMEX ENT TISSUE REMOVAL SYSTEM |
PROMEX, INC. |
| K022634 |
08/08/2002 |
CO-AXIAL INTRODUCER NEEDLE |
PROMEX, INC. |
| K973184 |
08/25/1997 |
PROSTATE SEEDING NEEDLE |
PROMEX, INC. |
| K993435 |
10/12/1999 |
MANUAL BONE MARROW BIOPSY DEVICE |
PROMEX, INC. |
| K023450 |
10/15/2002 |
BIOPSY SITE TISSUE MARKER DEVICE |
PROMEX, INC. |
| K955168 |
11/13/1995 |
SURGICAL CUTTER |
PROMEX, INC. |
| K994272 |
12/20/1999 |
AUTOMATED CORE BIOPSY DEVICE |
PROMEX, INC. |
| K961078 |
03/18/1996 |
AUTOMATED VITRECTOMY DEVICE |
PROMEX, INC. |
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