BABY TEETHER, MODEL 20104— 510(k) K014023

Name: FDA 510(k) clearance K014023
Creator: U.S. Food and Drug Administration
Published: 2002-08-02

Substantially Equivalent

Angelina Trading, Inc.

FDA 510(k) clearance K014023 for BABY TEETHER, MODEL 20104, Substantially Equivalent on 2002-08-02. Applicant: Angelina Trading, Inc.. Device class: 2.

Clearance details

Applicant: Angelina Trading, Inc.
Product code: Code KKO
Device class: Class 2
Regulation: 21 CFR 872.5550
Advisory panel: Dental
Date received: 2001-12-06
Decision date: 2002-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.