# Kronus, Inc.

- Location (FDA's records): Star, ID
- FDA decisions: 9 (1989–2023): 8 510(k) clearances and 1 De Novo grant
- Names in FDA's records: Kronus, Inc. (5); Kronus (4)
- Product codes: JZO (4), PNI (2), OIF (2), PCG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K220085: KRONUS IA-2 Autoantibody (IA-2Ab) ELISA Kit (Aug 24, 2023)
- K180607: Steroid 21-Hydroxylase Antibody (21-OHAb) ELISA Kit (Nov 23, 2018)
- K171731: KRONUS IA-2 Autoantibody (IA-2Ab) ELISA Kit (Jan 19, 2018)
- K161951: KRONUS Aquaporin-4 Autoantibody (AQP4Ab) ELISA Assay (Jul 22, 2016)
- DEN150030: KRONUS Aquaporin-4 Autoantibody (AQP4Ab) ELISA Assay (Apr 25, 2016)
- K915428: Kronus Kalibre Thyroglobulin Antibody Eia Kit (Mar 30, 1992)
- K915429: Kronus Kalibre Thyroid Peroxidase Antibody Eia Kit (Mar 30, 1992)
- K894364: Modified Kronus Test Kit for Antibodies to (Tpo) (Jul 25, 1989)

Source page: https://510kreport.com/company/kronus