Class Class II

TELLTALE Electrosurgical Guidewire System (K252592)

K252592 2025-11-13 Traditional
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Description

TELLTALE Electrosurgical Guidewire System by Telltale, LLC, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252592
Clearance Date2025-11-13
Clearance TypeTraditional
Product CodeSGO
Regulation Number870.1254

Categories

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