K970663 is an FDA 510(k) clearance for the CT CELLULOSER TRIACETATE HOLLOW FIBER DIALYZER (CT-110G/CT-190G). This device is classified as a Hemodialyzer, Re-use, High Flux (Class II — Special Controls, product code MSF).
Submitted by Baxter Healthcare Corp (Mcgaw Park, US). The FDA issued a Cleared decision on January 11, 1998, 324 days after receiving the submission on February 21, 1997.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5860.
| 510(k) Number | K970663 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 21, 1997 |
| Decision Date | January 11, 1998 |
| Days to Decision | 324 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | MSF — Hemodialyzer, Re-use, High Flux |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5860 |