K933847 is an FDA 510(k) clearance for the HYS-SURGIFLATOR VP. This device is classified as a Insufflator, Hysteroscopic (Class II - Special Controls, product code HIG).
Submitted by W.O.M. World of Medicine GmbH (Washington, US). The FDA issued a Cleared decision on August 15, 1995, 739 days after receiving the submission on August 6, 1993.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.1700.
| 510(k) Number | K933847 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 06, 1993 |
| Decision Date | August 15, 1995 |
| Days to Decision | 739 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 |