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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.
 
DeviceImpella RP System
Generic NameTemporary non-roller type right heart support blood pump
Regulation Number870.4360
ApplicantAbiomed, Inc.
22 Cherry Hill Drive
Danvers, MA 01923
PMA NumberP170011
Supplement NumberS022
Date Received03/09/2020
Decision Date03/30/2020
Product Code PYX 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Upgrade the laser welding workstation and associated Computer Numeric Control (CNC) program for the manufacture of the Pump Housing Assembly of the Impella RP catheter.
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