FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Clearview Intracoronary Shunts

K Number: K253998 · Decision Jan 20, 2026
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
209
Review Days
39

Basic Information

Device Name
Clearview Intracoronary Shunts
K Number
K253998
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic, Inc.
Date Received
December 12, 2025
Decision Date
January 20, 2026
Product Code
DWF
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

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