K955433 is an FDA 510(k) clearance for the DURALASTIC SILICONE TUBING. This device is classified as a Accessories, Catheter (Class I - General Controls, product code KGZ).
Submitted by Allied Biomedical Corp. (Paso Robles, US). The FDA issued a Cleared decision on January 26, 1996, 59 days after receiving the submission on November 28, 1995.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4200.
| 510(k) Number | K955433 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 28, 1995 |
| Decision Date | January 26, 1996 |
| Days to Decision | 59 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | KGZ — Accessories, Catheter |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4200 |