Class Class II

PowerGlide Pro™ Midline Catheter (K240359)

K240359 2024-07-29 Traditional
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Description

PowerGlide Pro™ Midline Catheter by Becton, Dickinson and Company (Bard Access Systems, Inc.) — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240359
Clearance Date2024-07-29
Clearance TypeTraditional
Product CodeFOZ
Regulation Number880.5200

Categories

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