K982472 is an FDA 510(k) clearance for the GENICON TROCAR, a Cannula, Surgical, General & Plastic Surgery (Class I — General Controls, product code GEA), submitted by Genicon, LC (Orlando, US). The FDA issued a Cleared decision on February 4, 1999, 204 days after receiving the submission on July 15, 1998. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4800.
| 510(k) Number | K982472 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 15, 1998 |
| Decision Date | February 04, 1999 |
| Days to Decision | 204 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GEA — Cannula, Surgical, General & Plastic Surgery |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4800 |