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

Fogarty Thru-Lumen Embolectomy Catheter

K Number: K240078 · Decision Aug 28, 2024
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
136
Review Days
230

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Basic Information

Device Name
Fogarty Thru-Lumen Embolectomy Catheter
K Number
K240078
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Edwards Lifesciences, LLC
Date Received
January 11, 2024
Decision Date
August 28, 2024
Product Code
DXE
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
DXE Catheter, Embolectomy

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