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FDA 510(k) Applications Submitted by MAINE STANDARDS COMPANY, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110880
03/30/2011
VALIDATE (R) GC3 CALIBRATION VERIFICATION / LINEARITY TEST KIT
MAINE STANDARDS COMPANY, LLC
K142964
10/14/2014
VALIDATE Anemia Calibration Verification/ Linearity Test Kit
MAINE STANDARDS COMPANY, LLC
K163498
12/13/2016
VALIDATE Heparin Calibration Verification/Linearity Test Kit
MAINE STANDARDS COMPANY, LLC
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