K213987 is an FDA 510(k) clearance for the ARCHITECT HSV-1 IgG, ARCHITECT HSV-1 IgG Calibrator, ARCHITECT HSV-1 IgG Controls. This device is classified as a Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1 (Class II - Special Controls, product code MXJ).
Submitted by Biokit, S.A. (Lli?? D?Amunt, ES). The FDA issued a Cleared decision on September 20, 2023, 639 days after receiving the submission on December 20, 2021.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3305.