The following data is part of a premarket notification filed by Dumex Medical Surgical Products, Ltd. with the FDA for Dumex Iodoform Packing Strip.
| Device ID | K990332 |
| 510k Number | K990332 |
| Device Name: | DUMEX IODOFORM PACKING STRIP |
| Classification | Gauze, External (with Drug/biologic/animal Source Material) |
| Applicant | DUMEX MEDICAL SURGICAL PRODUCTS, LTD. 104 SHORTING ROAD Toronto, Ontario, CA M1s 3s4 |
| Contact | Sharmini Atheray |
| Correspondent | Sharmini Atheray DUMEX MEDICAL SURGICAL PRODUCTS, LTD. 104 SHORTING ROAD Toronto, Ontario, CA M1s 3s4 |
| Product Code | GER |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-02-03 |
| Decision Date | 1999-04-14 |