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

MODIFICATION TO ULTIMUM EV HEMOSTASIS INTRODUCER (22F)

K Number: K023447 · Decision Oct 31, 2002
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
93
Review Days
16

Basic Information

Device Name
MODIFICATION TO ULTIMUM EV HEMOSTASIS INTRODUCER (22F)
K Number
K023447
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ST. JUDE MEDICAL
Date Received
October 15, 2002
Decision Date
October 31, 2002
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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