CONCHASMART BREATHING CIRCUIT

Humidifier, Respiratory Gas, (direct Patient Interface)

TELEFLEX, INC.

The following data is part of a premarket notification filed by Teleflex, Inc. with the FDA for Conchasmart Breathing Circuit.

Pre-market Notification Details

Device IDK140556
510k NumberK140556
Device Name:CONCHASMART BREATHING CIRCUIT
ClassificationHumidifier, Respiratory Gas, (direct Patient Interface)
Applicant TELEFLEX, INC. 2917 WECK DR. Research Triangle Park,  NC  27709
ContactAmanda Webb
CorrespondentAmanda Webb
TELEFLEX, INC. 2917 WECK DR. Research Triangle Park,  NC  27709
Product CodeBTT  
CFR Regulation Number868.5450 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-03-05
Decision Date2014-09-24
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
24026704553888 K140556 000
24026704553840 K140556 000
24026704553802 K140556 000
24026704553789 K140556 000
44026704553615 K140556 000
40801902126533 K140556 000
40801902126526 K140556 000
40801902126519 K140556 000

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