K983889 is an FDA 510(k) clearance for the HYS-SURGIFLATOR 150P, a Insufflator, Hysteroscopic (Class II — Special Controls, product code HIG), submitted by W.O.M. World of Medicine GmbH (Mansfield, US). The FDA issued a Cleared decision on January 14, 1999, 73 days after receiving the submission on November 2, 1998. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.1700.
| 510(k) Number | K983889 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 02, 1998 |
| Decision Date | January 14, 1999 |
| Days to Decision | 73 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HIG — Insufflator, Hysteroscopic |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 884.1700 |