K113330 is an FDA 510(k) clearance for the CABLECAP, a Light, Surgical, Fiberoptic (Class II — Special Controls, product code FST), submitted by Sensormed (Knoxville, US). The FDA issued a Cleared decision on January 12, 2012, 59 days after receiving the submission on November 14, 2011. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4580.
| 510(k) Number | K113330 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 14, 2011 |
| Decision Date | January 12, 2012 |
| Days to Decision | 59 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FST — Light, Surgical, Fiberoptic |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4580 |