PULPDENT SNOOP

Device, Caries Detection

PULPDENT CORP.

The following data is part of a premarket notification filed by Pulpdent Corp. with the FDA for Pulpdent Snoop.

Pre-market Notification Details

Device IDK964430
510k NumberK964430
Device Name:PULPDENT SNOOP
ClassificationDevice, Caries Detection
Applicant PULPDENT CORP. 80 OAKLAND ST. P.O. BOX 780 Watertown,  MA  02471 -0780
ContactKenneth J Berk
CorrespondentKenneth J Berk
PULPDENT CORP. 80 OAKLAND ST. P.O. BOX 780 Watertown,  MA  02471 -0780
Product CodeLFC  
CFR Regulation Number872.1740 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-11-05
Decision Date1997-01-17

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