The following data is part of a premarket notification filed by Brady Medical Products Co. with the FDA for Transorb(tm) Ulcer & Wound Dressing.
| Device ID | K922666 |
| 510k Number | K922666 |
| Device Name: | TRANSORB(TM) ULCER & WOUND DRESSING |
| Classification | Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic |
| Applicant | BRADY MEDICAL PRODUCTS CO. 727 W. GLENDALE AVE. P.O. BOX 571 Milwaukee, WI 53201 |
| Contact | W. K Reams |
| Correspondent | W. K Reams BRADY MEDICAL PRODUCTS CO. 727 W. GLENDALE AVE. P.O. BOX 571 Milwaukee, WI 53201 |
| Product Code | MGQ |
| 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 | 1992-05-28 |
| Decision Date | 1992-11-23 |