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FDA 510(k)

ABCOR CARIES DETECTOR MONITOR

K-Number: K791133 · 1979-08-28

ApplicantAbcor, Inc.
Decision Date1979-08-28
Product CodeLFC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ABCOR CARIES DETECTOR MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Abcor, Inc.. It received FDA 510(k) clearance on 1979-08-28 under 510(k) number K791133. 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 ABCOR CARIES DETECTOR MONITOR?

ABCOR CARIES DETECTOR MONITOR is a medical device that received FDA 510(k) clearance on 1979-08-28. The listed applicant is Abcor, Inc.. The 510(k) number is K791133.

When did ABCOR CARIES DETECTOR MONITOR receive FDA 510(k) clearance?

ABCOR CARIES DETECTOR MONITOR received FDA 510(k) clearance on 1979-08-28, under 510(k) number K791133.

Who is the listed applicant for ABCOR CARIES DETECTOR MONITOR?

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

What is the FDA product code for ABCOR CARIES DETECTOR MONITOR?

The FDA product code for ABCOR CARIES DETECTOR MONITOR is LFC.

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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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