Class Class II

OPTRELL™ Mapping Catheter with TRUEref™ Technology (K230253)

K230253 2023-03-02 Special
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Description

OPTRELL™ Mapping Catheter with TRUEref™ Technology by Biosense Webster, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230253
Clearance Date2023-03-02
Clearance TypeSpecial
Product CodeMTD
Regulation Number870.1220

Categories

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