CIDEX ACTIVATED DIALDEHYDE SOLUTION

Disinfectant, Medical Devices

JOHNSON & JOHNSON MEDICAL, INC.

The following data is part of a premarket notification filed by Johnson & Johnson Medical, Inc. with the FDA for Cidex Activated Dialdehyde Solution.

Pre-market Notification Details

Device IDK924434
510k NumberK924434
Device Name:CIDEX ACTIVATED DIALDEHYDE SOLUTION
ClassificationDisinfectant, Medical Devices
Applicant JOHNSON & JOHNSON MEDICAL, INC. P.O. BOX 90130 Arlington,  TX  76004 -3130
ContactWendt
CorrespondentWendt
JOHNSON & JOHNSON MEDICAL, INC. P.O. BOX 90130 Arlington,  TX  76004 -3130
Product CodeLRJ  
CFR Regulation Number880.6890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-09-01
Decision Date1994-03-29

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