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

MEDAMICUS AXIA RSN

K Number: K020563 · Decision May 21, 2002
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
20
Review Days
90

Basic Information

Device Name
MEDAMICUS AXIA RSN
K Number
K020563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDAMICUS, INC.
Date Received
February 20, 2002
Decision Date
May 21, 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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K022689 MODIFICATION TO MEDAMICUS AXIA RSN
K021004 VALVED PEELABLE INTRODUCER
K013120 PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18
K011085 GUIDEWIRE INTRODUCER SAFETY NEEDLE
K000824 PERCUTANEOUS INTRODUCER, MODEL 10383-XXX
K994097 MEDAMICUS EPIDURAL INTRODUCER
K990705 MEDAMICUS COAXIAL INTRODUCER KIT, 10330-XXX, BOSTON SCIENTIFIC COAXIAL DILATOR SET
K965167 PERCUTANEOUS VENOUS INTRODUCER 10264
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