LA500 BLUE LIGHT— 510(k) K033201

Substantially Equivalent

Apoza Enterprise Co., Ltd.

FDA 510(k) clearance K033201 for LA500 BLUE LIGHT, Substantially Equivalent on 2003-12-02. Applicant: Apoza Enterprise Co., Ltd.. Device class: 2.

Clearance details

Applicant: Apoza Enterprise Co., Ltd.
Product code: Code EBZ
Device class: Class 2
Regulation: 21 CFR 872.6070
Advisory panel: Dental
Date received: 2003-10-02
Decision date: 2003-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei Hsien, TW

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.