K123262 is an FDA 510(k) clearance for the OPTIFLUX ULTRA DIALYZER, a Dialyzer, High Permeability With Or Without Sealed Dialysate System (Class II — Special Controls, product code KDI), submitted by Fresenius Medical Care North America (Waltham,, US). The FDA issued a Cleared decision on January 6, 2014, 445 days after receiving the submission on October 18, 2012. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5860.
| 510(k) Number | K123262 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 18, 2012 |
| Decision Date | January 06, 2014 |
| Days to Decision | 445 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | KDI — Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5860 |