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

SEAL-AWAY CS INTRODUCER KIT, MODELS 407514, 407515

K Number: K013029 · Decision Oct 9, 2001
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
105
Review Days
29

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Basic Information

Device Name
SEAL-AWAY CS INTRODUCER KIT, MODELS 407514, 407515
K Number
K013029
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
September 10, 2001
Decision Date
October 9, 2001
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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