Class Class II

PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch (K250275)

K250275 2025-10-28 Traditional
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Description

PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch by Baylis Medical Technologies, Inc., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250275
Clearance Date2025-10-28
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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