K-number	K232273
Device name	RM Electrode (RMH 23-01)
Applicant	Retmap, Inc.
Product code	HLZ
Device class	Class II
Decision date	Dec 7, 2023
Decision	Substantially Equivalent
Regulation	886.1220

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View the full FDA submission: accessdata.fda.gov

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RM Electrode (RMH 23-01)

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