K-number	K041704
Device name	NEWGEL AND NEWGEL PLUS E
Applicant	Newmedical Technology, Inc.
Product code	MDA
Device class	Class I
Decision date	Oct 17, 2005
Decision	Substantially Equivalent
Regulation	878.4025

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View the full FDA submission: accessdata.fda.gov

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NEWGEL AND NEWGEL PLUS E

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