FDA 510(k) Applications Submitted by Elizabeth Goldstein

FDA 510(k) Number	Submission Date	Device Name	Applicant
K131957	06/27/2013	MR810RESPIRATORY HUMIDIFIER, 900MR810 ADULT SINGLE LIMB CIRCUIT, 900MR810E ADULT DUAL LIMB CIRCUIT	FISHER & PAYKEL HEALTHCARE, LTD.
K132017	07/01/2013	HC550 RESPIRATORY HUMIDIFIER, ADULT VENTILATOR CIRCUIT	FISHER & PAYKEL HEALTHCARE, LTD.
K133666	11/29/2013	RT016 INSPIRATORY FILTER	FISHER & PAYKEL HEALTHCARE LTD.
K143646	12/22/2014	MR810 System, 900MR810 Adult Single Limb Circuit, 900MR810E Adult Dual Limb Circuit	Fisher & Paykel Healthcare Ltd