MODIFICATION TO AVEA VENTILATOR

Ventilator, Continuous, Facility Use

VIASYS RESPIRATORY CARE INC

The following data is part of a premarket notification filed by Viasys Respiratory Care Inc with the FDA for Modification To Avea Ventilator.

Pre-market Notification Details

Device IDK073069
510k NumberK073069
Device Name:MODIFICATION TO AVEA VENTILATOR
ClassificationVentilator, Continuous, Facility Use
Applicant VIASYS RESPIRATORY CARE INC 1100 BIRD CENTER DR. Palm Springs,  CA  92262
ContactTom Gutierrez
CorrespondentTom Gutierrez
VIASYS RESPIRATORY CARE INC 1100 BIRD CENTER DR. Palm Springs,  CA  92262
Product CodeCBK  
CFR Regulation Number868.5895 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-10-30
Decision Date2008-01-25
Summary:summary

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