K-number	K203793
Device name	RithmID-SD Steerable Diagnostic Electrophysiology Catheter
Applicant	Synaptic Medical Corporation
Product code	DRF
Device class	Class II
Decision date	Feb 14, 2022
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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RithmID-SD Steerable Diagnostic Electrophysiology Catheter

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