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 |