The following data is part of a premarket notification filed by Hamilton Industries, Inc. with the FDA for Medalist Examination Table.
| Device ID | K883680 |
| 510k Number | K883680 |
| Device Name: | MEDALIST EXAMINATION TABLE |
| Classification | Table, Examination, Medical, Powered |
| Applicant | HAMILTON INDUSTRIES, INC. P.O. BOX 137 Two Rivers, WI 54241 |
| Contact | H. L Bunke |
| Correspondent | H. L Bunke HAMILTON INDUSTRIES, INC. P.O. BOX 137 Two Rivers, WI 54241 |
| Product Code | LGX |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-29 |
| Decision Date | 1988-10-04 |