FDA 510(k) Applications Submitted by DAVID G DAVIS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K032113	07/09/2003	ACIS (AUTOMATED CELLULAR IMAGING SYSTEM)	CHROMA VISION MEDICAL SYSTEMS INC.
K012138	07/10/2001	MODIFICATION TO ACIS (AUTOMATED CELLULAR IMAGING SYSTEM)	CHROMAVISION MEDICAL SYSTEMS, INC.
K062581	08/31/2006	OLYMPUS TSH REAGENT, CALIBRATOR AND CONTROL AND AU3000I IMMUNOASSAY SYSTEM	OLYMPUS AMERICA, INC.
K141374	05/27/2014	BICARBONATE CALIBRATOR	BECKMAN COULTER IRELAND INC
K141388	05/27/2014	SYSTEM CALIBRATER	BECKMAN COULTER IRELAND INC
K131546	05/29/2013	AU BICARBONATE REAGENT	BECKMAN COULTER IRELAND INC
K112412	08/22/2011	AU5800(R) CHEMISTRY ANALYZER	BECKMAN COULTER, INC.
K130019	01/03/2013	J-SCREW COMPRESSION SCREW	COMPETITIVE ENGINEERING INC.
K041503	06/07/2004	HOVERJACK AIR PATIENT LIFT DEVICE	D.T. DAVIS ENTERPRISES LTD.