CAVITRON— 510(k) K812568

Substantially Equivalent

G-C Intl. Corp.

FDA 510(k) clearance K812568 for CAVITRON, Substantially Equivalent on 1981-09-25. Applicant: G-C Intl. Corp.. Device class: 2.

Clearance details

Applicant: G-C Intl. Corp.
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1981-09-09
Decision date: 1981-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.