The following data is part of a premarket notification filed by Stierlen-maquet Ag with the FDA for Mobile Operating Table Heidelbergs 1130.
| Device ID | K843134 |
| 510k Number | K843134 |
| Device Name: | MOBILE OPERATING TABLE HEIDELBERGS 1130 |
| Classification | Table, Operating-room, Electrical |
| Applicant | STIERLEN-MAQUET AG 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GDC |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-08-09 |
| Decision Date | 1984-09-07 |