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

Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter

K Number: K192558 · Decision Apr 6, 2020
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
1
Review Days
202

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Basic Information

Device Name
Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter
K Number
K192558
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mivi Neurovascular
Date Received
September 17, 2019
Decision Date
April 6, 2020
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
DQY Catheter, Percutaneous

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