PORT-A-BOUT 240

Regulator, Pressure, Gas Cylinder

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 Port-a-bout 240.

Pre-market Notification Details

Device IDK772216
510k NumberK772216
Device Name:PORT-A-BOUT 240
ClassificationRegulator, Pressure, Gas Cylinder
Applicant HUDSON OXYGEN THERAPY SALES CO. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeCAN  
CFR Regulation Number868.2700 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1977-12-02
Decision Date1978-01-05

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