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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