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FDA 510(k) Applications Submitted by Adele Bindon
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110019
01/03/2011
RESPIRATORY HUMIDIFER
FISHER & PAYKEL HEALTHCARE, LTD.
K173770
12/11/2017
OJR215 Pressure Relief Manifold
Fisher & Paykel Healthcare Limited
K034026
12/29/2003
RT 138 & RT 141 DUAL-HEATED NEONATAL BREATHING CIRCUITS
FISHER & PAYKEL HEALTHCARE, LTD.
K073706
12/31/2007
RESPIRATORY HUMIDIFIER, MODEL MR850
FISHER & PAYKEL HEALTHCARE, LTD.
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