# Cirrus Diagnostics, Inc.

- Location (FDA's records): Chester, NJ
- FDA decisions: 10 (1991–1992): 10 510(k) clearances
- Product codes: CGJ (1), DHA (1), JLW (1), CEP (1), KLI (1), DPO (1), CHH (1), CDP (1), JJQ (1), CEE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 Products Corp.: 3 (https://510kreport.com/company/diagnostic-products)

## Its most-cited devices
- K911796: Immulite (TM) HCG (1991), cited by 1
- K914833: Immulite Digoxin (1991), cited by 1
- K905215: Immulite (TM) Automated Immunoassay Analyzer (1991), cited by 1

## Recent decisions
- K921704: Immulite (R) FSH (Jun 9, 1992)
- K920411: Immulite HLH (Mar 11, 1992)
- K914833: Immulite Digoxin (Nov 22, 1991)
- K911796: Immulite (TM) HCG (Jun 20, 1991)
- K910677: Immulite (TM) T-Uptake (Apr 29, 1991)
- K910261: Immulite (TM) Total T4 (Apr 16, 1991)
- K905648: CRP Lipid Reagent Test Pack (Mar 6, 1991)
- K905214: Immulite (TM) Total T3 (Feb 1, 1991)

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