K042502 is an FDA 510(k) clearance for the 3 SERIES PHOTOTHERAPY CABINET, a Light, Ultraviolet, Dermatological (Class II — Special Controls, product code FTC), submitted by Daavlin Distributing Co. (Bryan, US). The FDA issued a Cleared decision on October 14, 2004, 30 days after receiving the submission on September 14, 2004. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4630.
| 510(k) Number | K042502 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 14, 2004 |
| Decision Date | October 14, 2004 |
| Days to Decision | 30 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTC — Light, Ultraviolet, Dermatological |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4630 |