LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC— 510(k) K014069

Name: FDA 510(k) clearance K014069
Creator: U.S. Food and Drug Administration
Published: 2002-06-10

Substantially Equivalent

Princeton BioMeditech Corp.

FDA 510(k) clearance K014069 for LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC, Substantially Equivalent on 2002-06-10. Applicant: Princeton BioMeditech Corp.. Device class: 2.

Clearance details

Applicant: Princeton BioMeditech Corp.
Product code: Code DIO
Device class: Class 2
Regulation: 21 CFR 862.3250
Advisory panel: Clinical Toxicology
Date received: 2001-12-10
Decision date: 2002-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monmouth Junction, NJ, US

Download summary PDF View on FDA.gov ↗

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