The following data is part of a premarket notification filed by Midmark Corp. with the FDA for Power Examination Table Model # 405.
| Device ID | K894144 |
| 510k Number | K894144 |
| Device Name: | POWER EXAMINATION TABLE MODEL # 405 |
| Classification | Table, Examination, Medical, Powered |
| Applicant | MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
| Contact | John Oldiges |
| Correspondent | John Oldiges MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
| Product Code | LGX |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-06-13 |
| Decision Date | 1989-08-28 |