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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