FDA 510(k) Applications Submitted by HOLLY CRESSMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090475	02/24/2009	VALIDATE CM2 CALIBRATION VERIFICATION / LINEARITY TEST SET, MODEL 402	MAINE STANDARDS CO.
K110880	03/30/2011	VALIDATE (R) GC3 CALIBRATION VERIFICATION / LINEARITY TEST KIT	MAINE STANDARDS COMPANY, LLC
K091225	04/27/2009	VALIDATE GC1, GC2, GC3 AND GC4 CALIBRATION VERIFICATION/LINEARITY TEST SET	MAINE STANDARDS CO.
K082067	07/22/2008	MSC LIPID CONTROL	MAINE STANDARDS CO.
K072246	08/13/2007	VALIDATE SP1 CALIBRATION VERIFICATION/LINEARITY TEST SET, MODEL 601	MAINE STANDARDS CO.
K062501	08/25/2006	VALIDATE THYROID CALIBRATION VERIFICATION / LINEARITY TEST SET, MODEL 901	MAINE STANDARDS CO.
K103271	11/05/2010	MSC LIPID CONTROL	MAINE STANDARDS CO.
K083891	12/29/2008	VALIDATE THYROID CALIBRATION VERIFICATION TEST SET, MODEL 901	MAINE STANDARDS CO.
K113524	11/29/2011	VALIDATE VIT D CALIBRATION VERIFICATION/ LINEARITY TEST KIT	MAINE STANDARDS CO.