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

MODIFICATION TO IVS INTRODUCER SET, MODEL 1003

K Number: K031583 · Decision Jun 16, 2003
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
3
Review Days
26

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Basic Information

Device Name
MODIFICATION TO IVS INTRODUCER SET, MODEL 1003
K Number
K031583
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Integrated Vascular Systems, Inc.
Date Received
May 21, 2003
Decision Date
June 16, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYB), ordered by most recent decision date.

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Other Clearances by Integrated Vascular Systems, Inc.

K Number Device Name
K030723 IVS INTRODUCER SET, MODEL 1003
K020879 IVS CLIP CLOSURE SYSTEM, MODEL 1002 (IVS CLIP APPLIER); IVS INTRUDUCER SET, MODEL 1001