K920890 is an FDA 510(k) clearance for the OPERATING TABLE SYSTEM-BETAMAQUET 1140, a Table, Operating-room, Ac-powered (Class I — General Controls, product code FQO), submitted by Stierlen-Maquet AG (West Germany, GR). The FDA issued a Cleared decision on July 2, 1992, 141 days after receiving the submission on February 12, 1992. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4960.
| 510(k) Number | K920890 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 12, 1992 |
| Decision Date | July 02, 1992 |
| Days to Decision | 141 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FQO — Table, Operating-room, Ac-powered |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4960 |