The following data is part of a premarket notification filed by Ohio Medical Instrument Co., Inc. with the FDA for Mayfield Table-electric.
| Device ID | K851021 |
| 510k Number | K851021 |
| Device Name: | MAYFIELD TABLE-ELECTRIC |
| Classification | Table, Operating-room, Electrical |
| Applicant | OHIO MEDICAL INSTRUMENT CO., INC. 315 WEST LIBERTY Cincinnati, OH 45214 |
| Contact | James L Day |
| Correspondent | James L Day OHIO MEDICAL INSTRUMENT CO., INC. 315 WEST LIBERTY Cincinnati, OH 45214 |
| Product Code | GDC |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-03-12 |
| Decision Date | 1985-05-21 |