K950602 is an FDA 510(k) clearance for the PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS. This device is classified as a Dialyzer, Capillary, Hollow Fiber (Class II - Special Controls, product code FJI).
Submitted by Reprocessing Products Corp (Tucson, US). The FDA issued a Cleared decision on November 30, 1995, 294 days after receiving the submission on February 9, 1995.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5820.
| 510(k) Number | K950602 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 09, 1995 |
| Decision Date | November 30, 1995 |
| Days to Decision | 294 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | FJI — Dialyzer, Capillary, Hollow Fiber |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.5820 |