Dumex Medical Surgical Products, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K992732 | STERILE WATER & STERILE 0.9% SODIUM CHLORIDE | April 20, 2000 |
| K993119 | STERILE HYDROGEL | November 23, 1999 |
| K990332 | DUMEX IODOFORM PACKING STRIP | April 14, 1999 |
| K980779 | THALAFIX NATURAL SEA SALT DRESSING | June 26, 1998 |
| K980861 | DUMEX PAK-ITS COTTON GAUZE PACKING IMPREGNATED WITH HYDROGEL | May 20, 1998 |
| K980863 | DUMEX PAK-ITS NON-WOVEN DRESSING IMPREGNATED SITH SODIUM CHLORIDE (HYPERTONIC) | May 11, 1998 |
| K980777 | DUMEX PAK-ITS-ABSORBASALT COTTON GAUZE PACKING | May 4, 1998 |
| K980791 | DUMEX PAK-ITS WOVEN RIBBON PACKING | April 29, 1998 |
| K960815 | DUPAD, DUPAD W/ABDOM. PAD, DUMEX ABDOM. PAD, COMBO DRESSING ROLL/COMBINE DRESSING ROLL | April 29, 1996 |
| K950132 | DUMEX WET DRESSINGS | March 1, 1995 |
| K946326 | DUTEX GAUZE BANDAGE | January 24, 1995 |
| K945830 | DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE) | January 11, 1995 |
| K941217 | DUPAQUE SPONGE | April 21, 1994 |