K934744 is an FDA 510(k) clearance for the MIDMARK MAGNUM GENERAL SURGICAL TABLE, a Table, Operating-room, Electrical (Class I — General Controls, product code GDC), submitted by Midmark Corp. (Versailles, US). The FDA issued a Cleared decision on March 28, 1994, 175 days after receiving the submission on October 4, 1993. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4960.
| 510(k) Number | K934744 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 04, 1993 |
| Decision Date | March 28, 1994 |
| Days to Decision | 175 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | GDC — Table, Operating-room, Electrical |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4960 |