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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
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