Class Class II

Nordica PV Cryo Mapping Catheter (K233900)

K233900 2024-09-06 Traditional
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Description

Nordica PV Cryo Mapping Catheter by Synaptic Medical Corporation — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233900
Clearance Date2024-09-06
Clearance TypeTraditional
Product CodeDRF
Regulation Number870.1220

Categories

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