FDA 510(k) Applications Submitted by RUSCH, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980870 |
03/04/1998 |
RUSCH SILICONE FOLEY CATHETER |
RUSCH, INC. |
| K970021 |
01/03/1997 |
RUSCH SUPRAPUBIC TRAY |
RUSCH, INC. |
| K963993 |
10/04/1996 |
RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET |
RUSCH, INC. |
| K955495 |
12/01/1995 |
RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE |
RUSCH, INC. |
| K955564 |
12/06/1995 |
RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILE |
RUSCH, INC. |
| K993194 |
09/23/1999 |
RUSCH MANUAL RESUSCITATOR BAG |
RUSCH, INC. |
| K993528 |
10/18/1999 |
RUSCH EMERGENCY MASK |
RUSCH, INC. |
| K963779 |
09/20/1996 |
RUSCH ENTERAL FEEDING TUBE |
RUSCH, INC. |
| K974419 |
11/24/1997 |
RUSCH SIMPLASTIC COUNCILL TIP CATHETER |
RUSCH, INC. |
| K010420 |
02/12/2001 |
RUSCH MMG/O'NEIL CATHETER |
RUSCH, INC. |
|
|
