FDA 510(k) Applications Submitted by WALLACH SURGICAL DEVICES, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020711 |
03/05/2002 |
WALLACH LOOP ELECTRODE |
WALLACH SURGICAL DEVICES, INC. |
| K000768 |
03/09/2000 |
WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR |
WALLACH SURGICAL DEVICES, INC. |
| K021224 |
04/17/2002 |
ENDOCERVICAL BLOCK NEEDLE |
WALLACH SURGICAL DEVICES, INC. |
| K991669 |
05/14/1999 |
PMS 750 FINGERSWITCH |
WALLACH SURGICAL DEVICES, INC. |
| K992736 |
08/13/1999 |
WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUM |
WALLACH SURGICAL DEVICES, INC. |
| K983208 |
09/14/1998 |
WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR |
WALLACH SURGICAL DEVICES, INC. |
| K983840 |
10/30/1998 |
WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED) |
WALLACH SURGICAL DEVICES, INC. |
| K984306 |
12/02/1998 |
`THE INSEMINATOR' (PROPOSED) |
WALLACH SURGICAL DEVICES, INC. |
| K963348 |
08/26/1996 |
WALLACH INTEGRATION UNIT |
WALLACH SURGICAL DEVICES, INC. |
| K963653 |
09/12/1996 |
WALLACH QUANTUM 2000 ELECTROSURGICAL SYSTEM |
WALLACH SURGICAL DEVICES, INC. |
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