K041005 is an FDA 510(k) clearance for the GAMBRO PRISMAFLEX AND GAMBRO PRISMAFLEX M60 & M100 SETS. This device is classified as a Dialyzer, High Permeability With Or Without Sealed Dialysate System (Class II - Special Controls, product code KDI).
Submitted by Gambro Renal Products (Lakewood, US). The FDA issued a Cleared decision on October 7, 2004, 171 days after receiving the submission on April 19, 2004.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5860.
| 510(k) Number | K041005 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 19, 2004 |
| Decision Date | October 07, 2004 |
| Days to Decision | 171 days |
| Submission Type | Abbreviated |
| 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 |