BONASIL A+ IMPRESSION MATERIALS

Material, Impression

DMP LTD

The following data is part of a premarket notification filed by Dmp Ltd with the FDA for Bonasil A+ Impression Materials.

Pre-market Notification Details

Device IDK102836
510k NumberK102836
Device Name:BONASIL A+ IMPRESSION MATERIALS
ClassificationMaterial, Impression
Applicant DMP LTD 2ND KM KALYVION AVENUE MARKOPOULO INDUSTRIAL ZONE Markopoulo,  GR 19003
ContactDimitris Prantsidis
CorrespondentDimitris Prantsidis
DMP LTD 2ND KM KALYVION AVENUE MARKOPOULO INDUSTRIAL ZONE Markopoulo,  GR 19003
Product CodeELW  
CFR Regulation Number872.3660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2010-09-29
Decision Date2011-01-13

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20843471153875 K102836 000
10843471152949 K102836 000
20843471152939 K102836 000
10843471152925 K102836 000
10843471152918 K102836 000
20843471152908 K102836 000
10843471152895 K102836 000
10843471152888 K102836 000
10843471147679 K102836 000
10843471152956 K102836 000
10843471152963 K102836 000
20843471153868 K102836 000
10843471153854 K102836 000
20843471153844 K102836 000
20843471153837 K102836 000
20843471153820 K102836 000
20843471153813 K102836 000
10843471153809 K102836 000
20843471152977 K102836 000
10840326406912 K102836 000

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