510(k) K964430

Device
PULPDENT SNOOP
Applicant
PULPDENT CORP.
510(k) number
K964430
Product code
LFC  
Decision
Substantially Equivalent (SESE)
Decision date
1997-01-17
Date received
1996-11-05
Regulation
872.1740
Classification name
Device, Caries Detection
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
KENNETH J BERK
Address
80 Oakland St. P.O. Box 780 Watertown MA US 02471 02471

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LFC  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K222560BlueCheck™ Caries Detection & MonitoringIncisive Technologies Pty, Ltd.2023-05-16
K200601LumiCare Caries Diagnostic RinseGreenMark Biomedical, Inc.2021-03-29
K193447Vista DyesInter-Med/Vista Dental Products2020-03-11
K102821DISCOVREDPhoenix Dental, Inc.2011-03-11
K060330SEE-IT CARIES DETECTORRonvig Dental Mfg. A/S2006-04-07
K030807CARIES INDICATORConfi-Dental Products Co.2003-06-09
K012733CARIES DETECTORKuraray Medical, Inc.2001-09-14
K994368AMERICAN DENTAL PRODUCTS CARIES-DETECTOR PLUSAmerican Dental Products, Inc.2000-03-14
K982105ORAL POTENTIAL METER (OPM)Pertec of Wisconsin, Inc.1998-09-16
K973200CARIES STAINParkell, Inc.1997-11-06
K963927TEAM CARIES INDICATORCentrix, Inc.1996-11-15
K955445CARIES FINDERDanville Engineering, Inc.1996-02-08
K953526SEEKUltradent Products, Inc.1995-09-05
K951813CARIES DETECTORKuraray Co.1995-07-11
K913405KAR-D-TEKGresco Products, Inc.1991-10-28

Legacy Summary#

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FDA Review#

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