EARLY DETECTOR— 510(k) K833369

Substantially Equivalent

Warner-Lambert Co.

FDA 510(k) clearance K833369 for EARLY DETECTOR, Substantially Equivalent on 1984-08-02. Applicant: Warner-Lambert Co.. Device class: 2.

Clearance details

Applicant: Warner-Lambert Co.
Product code: Code KHE
Device class: Class 2
Regulation: 21 CFR 864.6550
Advisory panel: Hematology
Date received: 1983-09-27
Decision date: 1984-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.