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

TITAN MICRO CATHETER, MODEL 105-5074-153; HD INJECTOR, MODEL 103-0305

K Number: K022003 · Decision Sep 13, 2002
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
51
Review Days
86

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Basic Information

Device Name
TITAN MICRO CATHETER, MODEL 105-5074-153; HD INJECTOR, MODEL 103-0305
K Number
K022003
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micro Therapeutics, Inc.
Date Received
June 19, 2002
Decision Date
September 13, 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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K Number Device Name
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K090046 CONCERTO DETACHABLE COIL SYSTEM
K081465 AXIUM DETACHABLE COIL SYSTEM
K060747 FX DETACHABLE COIL SYSTEM
K060625 NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR
K051990 ECHELON MICRO CATHETER
K051560 NEXUS DETACHABLE COIL, MULTI-DIAMETER CSR AND HELIX SUPER SOFT CSR
K051425 NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR
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