K-number	K232562
Device name	PowerWire Radiofrequency Guidewire Kit
Applicant	Baylis Medical Technologies, Inc.
Product code	PDU
Device class	Class II
Decision date	Feb 28, 2024
Decision	Unknown
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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PowerWire Radiofrequency Guidewire Kit

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