RODDER VOLUME VENTILATOR

Ventilator, Continuous, Facility Use

PHARMAQUEST CORP.

The following data is part of a premarket notification filed by Pharmaquest Corp. with the FDA for Rodder Volume Ventilator.

Pre-market Notification Details

Device IDK820248
510k NumberK820248
Device Name:RODDER VOLUME VENTILATOR
ClassificationVentilator, Continuous, Facility Use
Applicant PHARMAQUEST CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeCBK  
CFR Regulation Number868.5895 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-01-29
Decision Date1982-04-16

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