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

EXPORT CATHETER

K Number: K040869 · Decision Jun 1, 2004
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
85
Applicant Total
468
Review Days
60

Basic Information

Device Name
EXPORT CATHETER
K Number
K040869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC VASCULAR
Date Received
April 2, 2004
Decision Date
June 1, 2004
Product Code
QEZ
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
QEZ Aspiration Thrombectomy Catheter

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