The following data is part of a premarket notification filed by Anco Medical Reagents & Assoc. with the FDA for Sgot Reagent Set.
| Device ID | K820466 |
| 510k Number | K820466 |
| Device Name: | SGOT REAGENT SET |
| Classification | Diazo, Ast/sgot |
| Applicant | ANCO MEDICAL REAGENTS & ASSOC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CIQ |
| CFR Regulation Number | 862.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-02-22 |
| Decision Date | 1982-03-11 |