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FDA 510(k)

CARIES FINDER

K-Number: K955445 · 1996-02-08

ApplicantDanville Engineering, Inc.
Decision Date1996-02-08
Product CodeLFC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CARIES FINDER is the device name listed in this FDA 510(k) record. The listed applicant is Danville Engineering, Inc.. It received FDA 510(k) clearance on 1996-02-08 under 510(k) number K955445. The device is classified under product code LFC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARIES FINDER?

CARIES FINDER is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is Danville Engineering, Inc.. The 510(k) number is K955445.

When did CARIES FINDER receive FDA 510(k) clearance?

CARIES FINDER received FDA 510(k) clearance on 1996-02-08, under 510(k) number K955445.

Who is the listed applicant for CARIES FINDER?

The FDA 510(k) record lists Danville Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARIES FINDER?

The FDA product code for CARIES FINDER is LFC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Danville Engineering, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K970589MICROETCHER APK953504MICROPRIMEK902836MICROETCHER

Related Devices (Code: LFC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222560BlueCheck™ Caries Detection & MonitoringIncisive Technologies Pty, Ltd.K200601LumiCare Caries Diagnostic RinseGreenMark Biomedical, Inc.K193447Vista DyesInter-Med/Vista Dental ProductsK102821DISCOVREDPhoenix Dental, Inc.K060330SEE-IT CARIES DETECTORRonvig Dental Mfg. A/SK030807CARIES INDICATORConfi-Dental Products Co.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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