Submission Details
| 510(k) Number | K851382 FDA.gov |
| FDA Decision | Cleared SN |
| Date Received | April 08, 1985 |
| Decision Date | July 05, 1985 |
| Days to Decision | 88 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
K851382 is an FDA 510(k) clearance for the CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING, a Dressing, Wound, Occlusive (Class I — General Controls, product code NAD), submitted by Chesebrough-Pond'S U.S.A. Co. (Trumbull, US). The FDA issued a Cleared decision on July 5, 1985, 88 days after receiving the submission on April 8, 1985. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4020.
| 510(k) Number | K851382 FDA.gov |
| FDA Decision | Cleared SN |
| Date Received | April 08, 1985 |
| Decision Date | July 05, 1985 |
| Days to Decision | 88 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | NAD — Dressing, Wound, Occlusive |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4020 |