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

MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER

K Number: K953335 · Decision Jan 23, 1996
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
51
Review Days
190

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Basic Information

Device Name
MICRO THERAPEUTICS VARIABLE INFUSION LENGTH CATHETER
K Number
K953335
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micro Therapeutics, Inc.
Date Received
July 17, 1995
Decision Date
January 23, 1996
Product Code
FOZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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Other Clearances by Micro Therapeutics, Inc.

K Number Device Name
K113289 ORION MICRO CATHETER
K113454 14 WIRE STANDARD, 14 WIRE LS
K090870 ECHELON MICRO CATHETER, MODELS 105-5092-150SA, 145-5092-150SA AND 190-5092-150SA AND SYRINGE ADAPTER ACCESSORY
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
Search all 51 clearances from Micro Therapeutics, Inc. →