K121724 is an FDA 510(k) clearance for the ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2, a Light Source, Fiberoptic, Routine (Class II — Special Controls, product code FCW), submitted by Richard Wolf Medical Instruments Corp. (Vernon Hills, US). The FDA issued a Cleared decision on September 20, 2012, 100 days after receiving the submission on June 12, 2012. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K121724 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 12, 2012 |
| Decision Date | September 20, 2012 |
| Days to Decision | 100 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FCW — Light Source, Fiberoptic, Routine |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |