QUICK CHECKER HCG PREGNANCY TEST— 510(k) K943859

Substantially Equivalent

Mizuho USA, Inc.

FDA 510(k) clearance K943859 for QUICK CHECKER HCG PREGNANCY TEST, Substantially Equivalent on 1995-02-10. Applicant: Mizuho USA, Inc..

Clearance details

Applicant: Mizuho USA, Inc.
Product code: Code JHI
Advisory panel: Clinical Chemistry
Date received: 1994-08-08
Decision date: 1995-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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Adverse events under product code JHI

product code JHI

Malfunction: 1,055
Total: 1,055

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.