K993625 is an FDA 510(k) clearance for the INSUFFLATION NEEDLE- 120MM, MODEL 900-200. This device is classified as a Insufflator, Laparoscopic (Class II - Special Controls, product code HIF).
Submitted by Genicon, LC (Orlando, US). The FDA issued a Cleared decision on June 20, 2000, 238 days after receiving the submission on October 26, 1999.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.1730.
| 510(k) Number | K993625 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 26, 1999 |
| Decision Date | June 20, 2000 |
| Days to Decision | 238 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HIF — Insufflator, Laparoscopic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.1730 |