The following data is part of a premarket notification filed by Diagnostic Solutions, Inc. with the FDA for Reagent For Determ. Potassium/in Human.
| Device ID | K800692 |
| 510k Number | K800692 |
| Device Name: | REAGENT FOR DETERM. POTASSIUM/IN HUMAN |
| Classification | Electrode, Ion Specific, Potassium |
| Applicant | DIAGNOSTIC SOLUTIONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CEM |
| CFR Regulation Number | 862.1600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-03-26 |
| Decision Date | 1980-05-28 |