K-number	K122562
Device name	E-TENG MODEL EOR 1
Applicant	E-Teng Technology, Inc.
Product code	IPL
Device class	Class II
Decision date	Aug 9, 2013
Decision	Substantially Equivalent
Regulation	890.3900

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View the full FDA submission: accessdata.fda.gov

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E-TENG MODEL EOR 1

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