# Kronus Market Development Associates, Inc.

- Location (FDA's records): Boise, ID
- FDA decisions: 11 (2003–2014): 10 510(k) clearances and 1 De Novo grant
- Product codes: NST (2), NWG (2), JZO (2), PCG (1), PHF (1), OIF (1), PAF (1), OCN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Diagnostic Hybrids, Inc.: 1 (https://510kreport.com/company/diagnostic-hybrids)

## Its most-cited devices
- K032134: TSH Receptor Antibody (Trab) Coated Tube (CT) Assay Kit (2003), cited by 1

## Recent decisions
- DEN140001: Zinc Transporter 8 Antibody (ZNT8AB) Elisa Assay Kit (Aug 20, 2014)
- K121046: Steroid 21-Hydroxylase Antibody (21-Ohab) Ria Assay Kit (Dec 20, 2012)
- K111956: Kronus Voltage Gated Calcium Channel (VGCC) Antibody Ria Assay Kit (May 30, 2012)
- K080523: Kronus Blocking Acetylcholine Receptor Autoantibody (Achrab) Ria Assay Kit (Jun 17, 2008)
- K080159: Kronus TSH Receptor Autoantibody (Trab) Elisa Assay Kit (May 22, 2008)
- K073590: Kronus IA-2 Autoantibody Ria Assay Kit (Apr 10, 2008)
- K072135: Kronus Gad Autoantibody Elisa Assay Kit (Nov 7, 2007)
- K070183: Kronus Insulin Autoantibody (Iaa) Assay Kit (Jul 13, 2007)

Source page: https://510kreport.com/company/kronus-market-development-associates