REVOTEK LC— 510(k) K012542

Substantially Equivalent

GC America, Inc.

FDA 510(k) clearance K012542 for REVOTEK LC, Substantially Equivalent on 2001-10-16. Applicant: GC America, Inc.. Device class: 2.

Clearance details

Applicant: GC America, Inc.
Product code: Code EBC
Device class: Class 2
Regulation: 21 CFR 872.3765
Advisory panel: Dental
Date received: 2001-08-07
Decision date: 2001-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alsip, IL, US

Download summary PDF View on FDA.gov ↗

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