510(k) K260163

AuST CSP Introducer by CenterPoint Systems, LLC — Product Code DYB

K260163 is an FDA 510(k) premarket notification submitted by CenterPoint Systems, LLC for the device "AuST CSP Introducer". The FDA issued a decision of Substantially Equivalent on February 19, 2026. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. CenterPoint Systems, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 19, 2026
Date Received
January 20, 2026
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Introducer, Catheter
Device Class
Class II
Regulation Number
870.1340
Review Panel
CV
Submission Type