QUIDEL HELICOBACTER PYLORI MICROWELL EIA TEST— 510(k) K912442

Substantially Equivalent

Quidel Corp.

FDA 510(k) clearance K912442 for QUIDEL HELICOBACTER PYLORI MICROWELL EIA TEST, Substantially Equivalent on 1991-09-16. Applicant: Quidel Corp..

Clearance details

Applicant: Quidel Corp.
Product code: Code LYR
Advisory panel: Microbiology
Date received: 1991-06-03
Decision date: 1991-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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Adverse events under product code LYR

product code LYR

Other: 1
Total: 1

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.