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

CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W

K Number: K031922 · Decision Oct 1, 2003
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
112
Review Days
100

Basic Information

Device Name
CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W
K Number
K031922
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MERIT MEDICAL SYSTEMS, INC.
Date Received
June 23, 2003
Decision Date
October 1, 2003
Product Code
DYB
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
DYB Introducer, Catheter

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