Class Class II

Accusafe Transseptal Guidewire (GTR31180, GTR31230) (K240246)

K240246 2024-07-26 Traditional
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Description

Accusafe Transseptal Guidewire (GTR31180, GTR31230) by Synaptic Medical Corporation — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240246
Clearance Date2024-07-26
Clearance TypeTraditional
Product CodeDRC
Regulation Number870.1390

Categories

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