ACCUSCREEN ASSAY— 510(k) K920018

Substantially Equivalent

Jk Research

FDA 510(k) clearance K920018 for ACCUSCREEN ASSAY, Substantially Equivalent on 1992-03-19. Applicant: Jk Research. Device class: 2.

Clearance details

Applicant: Jk Research
Product code: Code DKZ
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 1992-01-02
Decision date: 1992-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Auburn, CA, US

Download summary PDF View on FDA.gov ↗

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