K951907 is an FDA 510(k) clearance for the NAVARRE LOCKING PIGTAIL UNIVERSAL DRAINAGE CATHETER. This device is classified as a Catheter, Irrigation (Class I - General Controls, product code GBX).
Submitted by Navarre Biomedical , Ltd. (Plymouth, US). The FDA issued a Cleared decision on May 15, 1995, 21 days after receiving the submission on April 24, 1995.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4200.
| 510(k) Number | K951907 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 24, 1995 |
| Decision Date | May 15, 1995 |
| Days to Decision | 21 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GBX — Catheter, Irrigation |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4200 |