K-number	K221210
Device name	PainShield MD PLUS
Applicant	Nanovibronix, Inc.
Product code	PFW
Device class	Class II
Decision date	Nov 23, 2022
Decision	Substantially Equivalent
Regulation	890.5300

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Source

View the full FDA submission: accessdata.fda.gov

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PainShield MD PLUS

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