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

Hansen Medical Magellan Robotic Catheter 6Fr and Accessory Components

K Number: K151463 · Decision Aug 18, 2015
Classifications
1
FEI Numbers
46
Registration Numbers
47
Same Product Code
40
Applicant Total
14
Review Days
78

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Basic Information

Device Name
Hansen Medical Magellan Robotic Catheter 6Fr and Accessory Components
K Number
K151463
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1280
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hansen Medical, Inc.
Date Received
June 1, 2015
Decision Date
August 18, 2015
Product Code
DRA
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
DRA Catheter, Steerable

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Other Clearances by Hansen Medical, Inc.

K Number Device Name
K160919 Hansen Medical Magellan Robotic Catheter 9Fr
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K151730 Magellan Robotic System
K143227 Magellan Robotic System, Magellan Robotic Catheter 10Fr
K132369 MAGELLAN ROBOTIC SYSTEM, MAGELLAN ROBOTIC CATHETER 9FR
K111004 HANSEN MEDICAL VASCULAR CATHETER CONTROL SYSTEM AND CATHETER
K102168 SENSEI X ROBOTIC CATHETER SYSTEM
K091808 SENSEI ROBOTIC CATHETER SYSTEM, MODEL 02057
K090365 HANSEN MEDICAL ARTISAN S CONTROL CATHETER
K082075 HANSEN MEDICAL DILATOR FOR ARTISAN CONTROL CATHETER
Search all 14 clearances from Hansen Medical, Inc. →