E-TENG MODEL EOR 1— 510(k) K122562

Substantially Equivalent

E-Teng Technology, Inc.

FDA 510(k) clearance K122562 for E-TENG MODEL EOR 1, Substantially Equivalent on 2013-08-09. Applicant: E-Teng Technology, Inc.. Device class: 2.

Clearance details

Applicant: E-Teng Technology, Inc.
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 2012-08-22
Decision date: 2013-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung, TW

Download summary PDF View on FDA.gov ↗

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