CDR - PAN MODEL 4700— 510(k) K982661

Substantially Equivalent

Schick Technologies, Inc.

FDA 510(k) clearance K982661 for CDR - PAN MODEL 4700, Substantially Equivalent on 1998-12-11. Applicant: Schick Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Schick Technologies, Inc.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 1998-07-30
Decision date: 1998-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island, 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.