K945909 is an FDA 510(k) clearance for the NAVARRE N-FUSER(TM) PERIPHERAL INFUSION CATHETER. This device is classified as a Catheter, Continuous Flush (Class II - Special Controls, product code KRA).
Submitted by Navarre Biomedical , Ltd. (Plymouth, US). The FDA issued a Cleared decision on June 2, 1995, 182 days after receiving the submission on December 2, 1994.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1210.
| 510(k) Number | K945909 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 02, 1994 |
| Decision Date | June 02, 1995 |
| Days to Decision | 182 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | KRA — Catheter, Continuous Flush |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1210 |