K132551 is an FDA 510(k) clearance for the ZF 720, a Light, Surgical, Ceiling Mounted (Class II — Special Controls, product code FSY), submitted by Umbel Corporation (Diamond Bar, US). The FDA issued a Cleared decision on June 30, 2014, 320 days after receiving the submission on August 14, 2013. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4580.
| 510(k) Number | K132551 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 14, 2013 |
| Decision Date | June 30, 2014 |
| Days to Decision | 320 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FSY — Light, Surgical, Ceiling Mounted |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4580 |