The following data is part of a premarket notification filed by Icl Scientific with the FDA for Histimune Enzyme-ana Test.
| Device ID | K822346 |
| 510k Number | K822346 |
| Device Name: | HISTIMUNE ENZYME-ANA TEST |
| Classification | Antinuclear Antibody (enzyme-labeled), Antigen, Controls |
| Applicant | ICL SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LJM |
| CFR Regulation Number | 866.5100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-08-06 |
| Decision Date | 1982-10-08 |