PMH 1000 HEATED HUMIDIFIER

Humidifier, Respiratory Gas, (direct Patient Interface)

PEGASUS RESEARCH CORP.

The following data is part of a premarket notification filed by Pegasus Research Corp. with the FDA for Pmh 1000 Heated Humidifier.

Pre-market Notification Details

Device IDK013856
510k NumberK013856
Device Name:PMH 1000 HEATED HUMIDIFIER
ClassificationHumidifier, Respiratory Gas, (direct Patient Interface)
Applicant PEGASUS RESEARCH CORP. 1714 SOUTH LYON ST. Santa Ana,  CA  92705
ContactKenneth G Miller
CorrespondentKenneth G Miller
PEGASUS RESEARCH CORP. 1714 SOUTH LYON ST. Santa Ana,  CA  92705
Product CodeBTT  
CFR Regulation Number868.5450 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-11-06
Decision Date2003-02-21

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