510(k) K172980

Micropuncture Pedal Access Set by Cook Incorporated — Product Code DYB

K172980 is an FDA 510(k) premarket notification submitted by Cook Incorporated for the device "Micropuncture Pedal Access Set". The FDA issued a decision of Substantially Equivalent on May 3, 2018. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Cook Incorporated has 174 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 3, 2018
Date Received
Sep 27, 2017
Clearance Type
Traditional
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
510(k)