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

IVS INTRODUCER SET, MODEL 1003

K Number: K030723 · Decision Apr 3, 2003
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
3
Review Days
27

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
IVS INTRODUCER SET, MODEL 1003
K Number
K030723
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Integrated Vascular Systems, Inc.
Date Received
March 7, 2003
Decision Date
April 3, 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.

View all

Other Clearances by Integrated Vascular Systems, Inc.

K Number Device Name
K031583 MODIFICATION TO IVS INTRODUCER SET, MODEL 1003
K020879 IVS CLIP CLOSURE SYSTEM, MODEL 1002 (IVS CLIP APPLIER); IVS INTRUDUCER SET, MODEL 1001