K-number	K192715
Device name	CRF Radiofrequency Ablation System
Applicant	Cambridge Interventional, LLC
Product code	GEI
Device class	Class II
Decision date	Jan 7, 2020
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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CRF Radiofrequency Ablation System

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