ABCOR CARIES DETECTOR MONITOR— 510(k) K791133

Substantially Equivalent

Abcor, Inc.

FDA 510(k) clearance K791133 for ABCOR CARIES DETECTOR MONITOR, Substantially Equivalent on 1979-08-28. Applicant: Abcor, Inc.. Device class: 2.

Clearance details

Applicant: Abcor, Inc.
Product code: Code LFC
Device class: Class 2
Regulation: 21 CFR 872.1740
Advisory panel: Dental
Date received: 1979-06-18
Decision date: 1979-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.