The following data is part of a premarket notification filed by Livonia Diagnostics, Inc. with the FDA for Total Calcium Reagent Set.
| Device ID | K843895 |
| 510k Number | K843895 |
| Device Name: | TOTAL CALCIUM REAGENT SET |
| Classification | Cresolphthalein Complexone, Calcium |
| Applicant | LIVONIA DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CIC |
| CFR Regulation Number | 862.1145 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-03 |
| Decision Date | 1984-10-30 |