EMIT QST ACETAMINOPHEN ASSAY— 510(k) K844962

Substantially Equivalent

Syva Co.

FDA 510(k) clearance K844962 for EMIT QST ACETAMINOPHEN ASSAY, Substantially Equivalent on 1985-01-18. Applicant: Syva Co..

Clearance details

Applicant: Syva Co.
Product code: Code LDP
Advisory panel: Clinical Toxicology
Date received: 1984-12-24
Decision date: 1985-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

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Adverse events under product code LDP

product code LDP

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.