The following data is part of a premarket notification filed by Livonia Diagnostics, Inc. with the FDA for Magnesium Reagent Set.
| Device ID | K843893 |
| 510k Number | K843893 |
| Device Name: | MAGNESIUM REAGENT SET |
| Classification | Photometric Method, Magnesium |
| Applicant | LIVONIA DIAGNOSTICS, INC. 33091 WEST EIGHT MILE RD. Livonia, MI 48152 |
| Contact | Walter H Lambert |
| Correspondent | Walter H Lambert LIVONIA DIAGNOSTICS, INC. 33091 WEST EIGHT MILE RD. Livonia, MI 48152 |
| Product Code | JGJ |
| CFR Regulation Number | 862.1495 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-03 |
| Decision Date | 1984-10-30 |