K-number	K061632
Device name	GLOBUS PREMIUM MUSCLE STIMULATOR
Applicant	Domino S.R.L.
Product code	NGX
Device class	Class II
Decision date	Apr 30, 2007
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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GLOBUS PREMIUM MUSCLE STIMULATOR

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