K-number	K192603
Device name	Spes Medica Subdermal Needle Electrodes
Applicant	Spes Medica Srl
Product code	GXZ
Device class	Class II
Decision date	Nov 22, 2019
Decision	Substantially Equivalent
Regulation	882.1350

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View the full FDA submission: accessdata.fda.gov

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Spes Medica Subdermal Needle Electrodes

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