K-number	K010265
Device name	BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265
Applicant	Baylis Medical Co., Inc.
Product code	GEI
Device class	Class II
Decision date	Apr 9, 2001
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265

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