K974426 is an FDA 510(k) clearance for the POTENCY TEST STRIPS, INDICATOR TEST STRIPS. This device is classified as a Dialyzer Reprocessing System (Class II - Special Controls, product code LIF).
Submitted by Reprocessing Products Corp (Maple Grove, US). The FDA issued a Cleared decision on February 10, 1999, 471 days after receiving the submission on October 27, 1997.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5820.
| 510(k) Number | K974426 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 27, 1997 |
| Decision Date | February 10, 1999 |
| Days to Decision | 471 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | LIF — Dialyzer Reprocessing System |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.5820 |