K940378 is an FDA 510(k) clearance for the COVERLET ADHESIVE DRESSING. This device is classified as a Tape And Bandage, Adhesive (Class I - General Controls, product code KGX).
Submitted by Beiersdorf, Inc. (Norwalk, US). The FDA issued a Cleared decision on July 29, 1994, 184 days after receiving the submission on January 26, 1994.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 880.5240.
| 510(k) Number | K940378 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - NSE Converted (SN) |
| Date Received | January 26, 1994 |
| Decision Date | July 29, 1994 |
| Days to Decision | 184 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | KGX — Tape And Bandage, Adhesive |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 880.5240 |