# King Diagnostics, Inc.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 41 (1981–1993): 41 510(k) clearances
- Product codes: JPA (3), JIS (2), KNK (2), CGA (2), CFR (2), CHH (2), CIG (1), CFJ (1), CHJ (1), CJE (1), CKA (1), CKE (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
- Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB: 1 (https://510kreport.com/company/gonotec-gesellschaft-fuer-mess-und-regeltechnik-mb)

## Its most-cited devices
- K931834: King Sodium/Potassium Standard Modified (1993), cited by 1

## Recent decisions
- K933329: King Diagnostics Iron and Total Iron Binding Capacity Reagent (Oct 22, 1993)
- K931834: King Sodium/Potassium Standard Modified (Aug 25, 1993)
- K931773: HDL Precipitating Reagent (Dextran Sulfate) (Aug 16, 1993)
- K931326: King Diagnostics CK Reagent (Jun 15, 1993)
- K923129: King Diagnostics Glucose (HK) Reagent (Nov 2, 1992)
- K922969: King Diagnostics Urea Nitrogen Reagent (Oct 13, 1992)
- K922921: King Diagnostics Chloride Reagent (Oct 5, 1992)
- K923927: King Diagnostics Magnesium Reagent (Sep 30, 1992)

Source page: https://510kreport.com/company/king-diagnostics