# Mizuho USA, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 7 (1993–2006): 7 510(k) clearances
- Product codes: LCX (5), DHA (1), JHI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K060825: Multi-Use Electronic Pregnancy Test (Jun 19, 2006)
- K043231: Proof Positive Electronic Pregnancy Test (Apr 25, 2005)
- K000844: Absolute HCG Pregnancy Test (Jun 16, 2000)
- K964002: Naturale HCG Pregnancy Tes (Nov 7, 1996)
- K943859: Quick Checker HCG Pregnancy Test (Feb 10, 1995)
- K945568: HCG Midstream Pregnancy Test (Jan 17, 1995)
- K931997: HCG Midstream Pregnancy Test (Sep 10, 1993)

Source page: https://510kreport.com/company/mizuho-usa