Cleared Traditional

LIFESIGN MET, STATUS STIK MET, ACCUSIGN STIK MET, ACCUSTIK MET, ACCUSIGN MET, STATUS DS MET

K014192 · Princeton BioMeditech Corp. · Toxicology
May 2002
Decision
153d
Days
—
Risk

About This 510(k) Submission

K014192 is an FDA 510(k) clearance for the LIFESIGN MET, STATUS STIK MET, ACCUSIGN STIK MET, ACCUSTIK MET, ACCUSIGN MET, STATUS DS MET, a Kit, Test, Multiple, Drugs Of Abuse, Over The Counter, submitted by Princeton BioMeditech Corp. (Monmouth Junction, US). The FDA issued a Cleared decision on May 23, 2002, 153 days after receiving the submission on December 21, 2001. This device falls under the Toxicology review panel.

Submission Details

510(k) Number K014192 FDA.gov
FDA Decision Cleared SESE
Date Received December 21, 2001
Decision Date May 23, 2002
Days to Decision 153 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF

Device Classification

Product Code MVO — Kit, Test, Multiple, Drugs Of Abuse, Over The Counter
Device Class —

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