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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceGALILEO INTRAVASCULAR RADIOTHERAPY SYSTEM
Classification Nameintravascular radiation delivery system
Generic Nameintravascular radiation delivery system
Applicant
GUIDANT CORP.
26531 ynez rd.
temecula, CA 92591-4630
PMA NumberP000052
Supplement NumberS010
Date Received07/05/2002
Decision Date08/02/2002
Product Code
MOU[ Registered Establishments with MOU ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
AMENDING IMPLEMENTATION OF MANUFACTURING CHANGES DESCRIBED IN P000052/S007, APPROVED APRIL 17, 2002 AND ADDING A VERIFICATION STEP TO THE PREVENTIVE MAINTENANCE CHECKLIST FOR THE GALILEO SOURCE DELIVERY UNIT.
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