CORPAK-MONITOR ENTERAL FEEDING CONTAIN

Tubes, Gastrointestinal (and Accessories)

CORPAK CO.

The following data is part of a premarket notification filed by Corpak Co. with the FDA for Corpak-monitor Enteral Feeding Contain.

Pre-market Notification Details

Device IDK821410
510k NumberK821410
Device Name:CORPAK-MONITOR ENTERAL FEEDING CONTAIN
ClassificationTubes, Gastrointestinal (and Accessories)
Applicant CORPAK CO. 4221 Richmond Rd., N.W. Walker,  MI  49534
Product CodeKNT  
CFR Regulation Number876.5980 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-05-14
Decision Date1982-05-24

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