CDR-CAM— 510(k) K963778

Substantially Equivalent

Schick Technologies, Inc.

FDA 510(k) clearance K963778 for CDR-CAM, Substantially Equivalent on 1996-11-22. Applicant: Schick Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Schick Technologies, Inc.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1996-09-20
Decision date: 1996-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island City, NY, 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.