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 Heated Humidifier.

Pre-market Notification Details

Device IDK983783
510k NumberK983783
Device Name:HEATED HUMIDIFIER
ClassificationHumidifier, Respiratory Gas, (direct Patient Interface)
Applicant PEGASUS RESEARCH CORP. 1714 SOUTH LYON ST. Santa Ana,  CA  92705
ContactE J Smith
CorrespondentE J Smith
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 Received1998-10-27
Decision Date2000-10-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.