# Quidel Cardiovascular, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 2 (2019–2020): 2 510(k) clearances
- Product codes: DKZ (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Immunalysis Corporation: 2 (https://510kreport.com/company/immunalysis)
- Biosite Incorporated: 2 (https://510kreport.com/company/biosite)
- Genprime, Inc.: 1 (https://510kreport.com/company/genprime)
- Microgenics Corp.: 1 (https://510kreport.com/company/microgenics)

## Its most-cited devices
- K182719: Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterPro (2019), cited by 1

## Recent decisions
- K200363: Quidel Triage® TOX Drug Screen, 94600 (Mar 11, 2020)
- K182719: Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterPro (Jun 19, 2019)

Source page: https://510kreport.com/company/quidel-cardiovascular