Class Class II

NUVISION™ NAV Ultrasound Catheter (K223766)

K223766 2023-02-16 Traditional
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Description

NUVISION™ NAV Ultrasound Catheter by Biosense Webster, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223766
Clearance Date2023-02-16
Clearance TypeTraditional
Product CodeOBJ
Regulation Number870.1200

Categories

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