Class Class II

Indigo® Aspiration System – Aspiration Catheter 6X (K242319)

K242319 2024-09-03 Special
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Description

Indigo® Aspiration System – Aspiration Catheter 6X by Penumbra, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242319
Clearance Date2024-09-03
Clearance TypeSpecial
Product CodeQEW
Regulation Number870.5150

Categories

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