K926496 is an FDA 510(k) clearance for the SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN. This device is classified as a Catheter, Irrigation (Class I - General Controls, product code GBX).
Submitted by Sil-Med Corp. (Taunton, US). The FDA issued a Cleared decision on May 24, 1995, 876 days after receiving the submission on December 29, 1992.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4200.
| 510(k) Number | K926496 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 29, 1992 |
| Decision Date | May 24, 1995 |
| Days to Decision | 876 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 |