VERASOFT ES

Alloy, Metal, Base

AALBA DENT, INC.

The following data is part of a premarket notification filed by Aalba Dent, Inc. with the FDA for Verasoft Es.

Pre-market Notification Details

Device IDK033356
510k NumberK033356
Device Name:VERASOFT ES
ClassificationAlloy, Metal, Base
Applicant AALBA DENT, INC. 400 WATT DR. Cordelia,  CA  94534
ContactVincent Benetti
CorrespondentVincent Benetti
AALBA DENT, INC. 400 WATT DR. Cordelia,  CA  94534
Product CodeEJH  
CFR Regulation Number872.3710 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-09-20
Decision Date2003-12-30

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
90852187007111 K033356 000

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