Rusch, Inc.
Rusch, Inc. appears in FDA public data with 0 recalls, 26 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 9, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 26
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K010420 | RUSCH MMG/O'NEIL CATHETER | May 9, 2001 |
| K993528 | RUSCH EMERGENCY MASK | May 31, 2000 |
| K993194 | RUSCH MANUAL RESUSCITATOR BAG | March 24, 2000 |
| K980870 | RUSCH SILICONE FOLEY CATHETER | June 9, 1998 |
| K974419 | RUSCH SIMPLASTIC COUNCILL TIP CATHETER | January 27, 1998 |
| K963779 | RUSCH ENTERAL FEEDING TUBE | May 23, 1997 |
| K970021 | RUSCH SUPRAPUBIC TRAY | February 7, 1997 |
| K963993 | RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET | December 17, 1996 |
| K955564 | RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILE | June 28, 1996 |
| K955495 | RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE | June 27, 1996 |
| K953963 | RUSCH SINGLE LUMEN BRONCHIAL TUVBE SET, STERILE, FOR LEFT & RIGHT SIDED BRONCHIAL INTUBATION | November 27, 1995 |
| K922567 | LOW PROFILE CATHETER | November 21, 1995 |
| K953593 | RUSCH TRACHEAL BRONCHIAL Y STENT | October 13, 1995 |
| K952100 | RUSCH ENDOTRACHEAL TUBE STYLET | August 8, 1995 |
| K952187 | RUSCH SUPRAFLEX SUPRAPUBIC CYSTOSTOMY CATHETER KIT, STERILE | July 25, 1995 |
| K935842 | RUSCH LASERTUBUS/RUSCH LASER RESISTANT CUFFED WITH MURPHY EYE | May 23, 1995 |
| K922998 | ENFUSE ENTERAL FEEDING TUBE | December 3, 1993 |
| K925507 | RUSCH SAFETY CLEAR UNCUFFED WITH MAGILL TIP | September 2, 1993 |
| K925508 | RUSCH SAFETY CLEAR PLUS CUFFED W/MAGILL TIP | September 2, 1993 |
| K925505 | RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE | September 2, 1993 |