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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.
 
DeviceTHERAPY ABLATION CATHETER
Generic NameCardiac ablation percutaneous catheter
ApplicantIrvine Biomedical, Inc.
2375 Morse Ave.
Irvine, CA 92614
PMA NumberP040014
Supplement NumberS015
Date Received11/16/2010
Decision Date01/11/2011
Product Code LPB 
Advisory Committee Cardiovascular
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR A DESIGN MODIFICATION TO THE TIP ELECTRODE STEM OUTER DIAMETER (OD) SO THAT THE GAP BETWEEN THE TIP ELECTRODE OD AND TUBE INSIDE DIAMETER (ID) IS REDUCED TO -0.0015¿ TO +0.0015¿ FROM -0.003¿ TO +0.003¿ FOR CONSISTENT GAP INTERFERENCE.
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