MDI ADAPTOR

Nebulizer (direct Patient Interface)

HUDSON OXYGEN THERAPY SALES CO.

The following data is part of a premarket notification filed by Hudson Oxygen Therapy Sales Co. with the FDA for Mdi Adaptor.

Pre-market Notification Details

Device IDK900783
510k NumberK900783
Device Name:MDI ADAPTOR
ClassificationNebulizer (direct Patient Interface)
Applicant HUDSON OXYGEN THERAPY SALES CO. 27711 DIAZ ST. P.O. BOX 66 Temecula,  CA  92390
ContactJorge Haider
CorrespondentJorge Haider
HUDSON OXYGEN THERAPY SALES CO. 27711 DIAZ ST. P.O. BOX 66 Temecula,  CA  92390
Product CodeCAF  
CFR Regulation Number868.5630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-02-20
Decision Date1990-07-18

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
14026704595546 K900783 000
24026704656930 K900783 000
24026704595543 K900783 000
24026704595093 K900783 000
24026704390223 K900783 000

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