IMPREGUM GARANT L DUOSOFT

Material, Impression

ESPE DENTAL AG

The following data is part of a premarket notification filed by Espe Dental Ag with the FDA for Impregum Garant L Duosoft.

Pre-market Notification Details

Device IDK994190
510k NumberK994190
Device Name:IMPREGUM GARANT L DUOSOFT
ClassificationMaterial, Impression
Applicant ESPE DENTAL AG ESPE PLATZ Seefeld, Bavaria,  DE D-82229
ContactAndreras Petermann
CorrespondentAndreras Petermann
ESPE DENTAL AG ESPE PLATZ Seefeld, Bavaria,  DE D-82229
Product CodeELW  
CFR Regulation Number872.3660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-12-13
Decision Date2000-01-27
Summary:summary

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