Class Class II

PowerWire® 14 Radiofrequency Guidewire Kit (K251158)

K251158 2025-09-11 Traditional
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Description

PowerWire® 14 Radiofrequency Guidewire Kit by Baylis Medical Technologies, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251158
Clearance Date2025-09-11
Clearance TypeTraditional
Product CodePDU
Regulation Number870.1250

Categories

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