The following data is part of a premarket notification filed by Smith & Nephew Richards, Inc. with the FDA for Nasal Cavity Wound Dressing.
| Device ID | K923957 |
| 510k Number | K923957 |
| Device Name: | NASAL CAVITY WOUND DRESSING |
| Classification | Bandage, Liquid |
| Applicant | SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
| Contact | Jeff Cobb |
| Correspondent | Jeff Cobb SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-06 |
| Decision Date | 1993-05-05 |