Submission Details
| 510(k) Number | K931933 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 19, 1993 |
| Decision Date | July 08, 1993 |
| Days to Decision | 80 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
K931933 is an FDA 510(k) clearance for the CHAD LABS ADHESIVE BANDAGE REMOVER, a Solvent, Adhesive Tape (Class I — General Controls, product code KOX), submitted by Chad Labs Corp. (Milford, US). The FDA issued a Cleared decision on July 8, 1993, 80 days after receiving the submission on April 19, 1993. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4730.
| 510(k) Number | K931933 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 19, 1993 |
| Decision Date | July 08, 1993 |
| Days to Decision | 80 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | KOX — Solvent, Adhesive Tape |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4730 |