K-number	K190256
Device name	Rulo Radiofrequency Lesion Probe
Applicant	Epimed International, Inc.
Product code	GXI
Device class	Class II
Decision date	Mar 8, 2019
Decision	Substantially Equivalent
Regulation	882.4725

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Source

View the full FDA submission: accessdata.fda.gov

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Rulo Radiofrequency Lesion Probe

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