FDA 510(k) Applications Submitted by DELTEX MEDICAL LIMITED

FDA 510(k) Number	Submission Date	Device Name	Applicant
K172457	08/14/2017	Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM	Deltex Medical Limited
K111542	06/02/2011	DELTEX MEDICAL CARDIOQ EDM	DELTEX MEDICAL LIMITED
K073593	12/21/2007	I2S DOPPLER PROBE ( 6 HOUR), I2S DOPPLER PROBE (24 HOUR), I2C DOPPLER PROBE (72 HOUR), MODELS 9090-7015, 9090-7016	DELTEX MEDICAL LIMITED
K150347	02/11/2015	Deltex Medical CardioQ-EDM, Deltex Medical CardioQ-EDM+	DELTEX MEDICAL LIMITED
K142932	10/09/2014	Deltex Medical KDP72 Doppler Probe	DELTEX MEDICAL LIMITED
K132139	07/11/2013	DELTEX MEDICAL CARDIOQ-EDM+	DELTEX MEDICAL LIMITED