The following data is part of a premarket notification filed by Midmark Corp. with the FDA for Midmark Magnum General Surgical Table.
| Device ID | K934744 |
| 510k Number | K934744 |
| Device Name: | MIDMARK MAGNUM GENERAL SURGICAL TABLE |
| Classification | Table, Operating-room, Electrical |
| Applicant | MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
| Contact | Bradley K Seiden |
| Correspondent | Bradley K Seiden MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
| Product Code | GDC |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-10-04 |
| Decision Date | 1994-03-28 |