K992540 is an FDA 510(k) clearance for the XENON LIGHT SOURCE PES 1, a Light Source, Endoscope, Xenon Arc (Class II — Special Controls, product code GCT), submitted by Laser Optik Systeme GmbH & Co. KG (Germany, DE). The FDA issued a Cleared decision on September 14, 1999, 47 days after receiving the submission on July 29, 1999. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K992540 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 29, 1999 |
| Decision Date | September 14, 1999 |
| Days to Decision | 47 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | GCT — Light Source, Endoscope, Xenon Arc |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |