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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.
 
DeviceMAGNETOM
Generic NameSystem, nuclear magnetic resonance imaging
Regulation Number892.1000
ApplicantSiemens Corp.
186 Wood Ave. S.
Iselin, NJ 08830
PMA NumberP830081
Supplement NumberS007
Date Received03/21/1986
Decision Date06/03/1986
Product Code LNH 
Advisory Committee Radiology
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
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