K955439 is an FDA 510(k) clearance for the THE REEL THING (MODIFICATION), a Catheter, Irrigation (Class I — General Controls, product code GBX), submitted by Biomedical Devices, Inc. (Irvine, US). The FDA issued a Cleared decision on December 26, 1995, 43 days after receiving the submission on November 13, 1995. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4200.
| 510(k) Number | K955439 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 13, 1995 |
| Decision Date | December 26, 1995 |
| Days to Decision | 43 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | GBX — Catheter, Irrigation |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4200 |