HYDROGUM

Material, Impression

ZHERMACK DENTAL PRODUCTION

The following data is part of a premarket notification filed by Zhermack Dental Production with the FDA for Hydrogum.

Pre-market Notification Details

Device IDK935898
510k NumberK935898
Device Name:HYDROGUM
ClassificationMaterial, Impression
Applicant ZHERMACK DENTAL PRODUCTION 7527 WESTMORELAND AVE. St. Louis,  MO  63105
ContactEvan C Dick, Ph.d.
CorrespondentEvan C Dick, Ph.d.
ZHERMACK DENTAL PRODUCTION 7527 WESTMORELAND AVE. St. Louis,  MO  63105
Product CodeELW  
CFR Regulation Number872.3660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-10-12
Decision Date1995-08-22

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