FDA 510(k) Applications Submitted by BRETT WHISTON
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K060044 |
01/06/2006 |
ACUTE CARE FACE MASK, MODEL RT040 |
FISHER & PAYKEL HEALTHCARE, LTD. |
K020332 |
01/31/2002 |
RESPIRATORY HUMIDIFIER, MODEL MR850 |
FISHER & PAYKEL HEALTHCARE, LTD. |
K131895 |
06/25/2013 |
AIRVO 2 HUMIDIFIER, MYAIRVO 2 HUMIDIFIER |
FISHER & PAYKEL HEALTHCARE, LTD. |
K121975 |
07/05/2012 |
AIRVO HUMIDIFIER MYAIRO HUMIDIFIER |
FISHER & PAYKEL HEALTHCARE, LTD. |
K002414 |
08/07/2000 |
PHOTOTHERAPY LAMP 900IW501JE PHOTOTHERAPY POWER MODULE 900IW502JE |
FISHER & PAYKEL HEALTHCARE, LTD. |
K033710 |
11/26/2003 |
MR850 RESPIRATORY HUMIDIFIER, MODEL MR850JHU |
FISHER & PAYKEL HEALTHCARE, LTD. |
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