The following data is part of a premarket notification filed by Stierlen-maquet Ag with the FDA for Operating Table System-betamaquet 1140.
| Device ID | K920890 |
| 510k Number | K920890 |
| Device Name: | OPERATING TABLE SYSTEM-BETAMAQUET 1140 |
| Classification | Table, Operating-room, Ac-powered |
| Applicant | STIERLEN-MAQUET AG KEHLER STRASSE 31 7550 RASTATT West Germany, GR |
| Contact | Bastert |
| Correspondent | Bastert STIERLEN-MAQUET AG KEHLER STRASSE 31 7550 RASTATT West Germany, GR |
| Product Code | FQO |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-12 |
| Decision Date | 1992-07-02 |