# Rapid Diagnostics, Inc.

- Location (FDA's records): Burlingame, CA
- FDA decisions: 4 (1998–2004): 4 510(k) clearances
- Product codes: DKZ (2), JHI (1), DJG (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
- Mp Biomedicals, LLC: 3 (https://510kreport.com/company/mp-biomedicals)

## Its most-cited devices
- K033566: Micromedic Drugs of Abuse Panel Test (9), Catalog Number 07RD-7062 (2004), cited by 2
- K003809: Rapid Drugs of Abuse Single and Multiple Test Panels (2001), cited by 1

## Recent decisions
- K033566: Micromedic Drugs of Abuse Panel Test (9), Catalog Number 07RD-7062 (May 17, 2004)
- K020716: Rapid Opiates Test Strip II, Rapid Opiates Test Card II and Doa Multiple Drug Test Cards (UP to Six Tests) (May 6, 2002)
- K003809: Rapid Drugs of Abuse Single and Multiple Test Panels (Apr 20, 2001)
- K981770: Rapidhcg Pregnancy Test (Jun 5, 1998)

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