FREEDOM, MODEL 4660— 510(k) K001023

Name: FDA 510(k) clearance K001023
Creator: U.S. Food and Drug Administration
Published: 2000-09-22

Substantially Equivalent

Johnson & Johnson Consumer Companies, Inc.

FDA 510(k) clearance K001023 for FREEDOM, MODEL 4660, Substantially Equivalent on 2000-09-22. Applicant: Johnson & Johnson Consumer Companies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Johnson & Johnson Consumer Companies, Inc.
Product code: Code SEJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2000-03-30
Decision date: 2000-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skillman, NJ, US

Download summary PDF View on FDA.gov ↗

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