MAGNETOM

FDA Premarket Approval P830081 S001

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.

Pre-market Approval Supplement Details

DeviceMAGNETOM
Generic NameSystem, Nuclear Magnetic Resonance Imaging
ApplicantSIEMENS CORP.
Date Received1984-12-07
Decision Date1985-07-10
PMAP830081
SupplementS001
Product CodeLNH 
Advisory CommitteeRadiology
Expedited ReviewNo
Combination Product No
Applicant Address SIEMENS CORP. 186 Wood Ave., South iselin, NJ 08830

Supplemental Filings

Supplement NumberDateSupplement Type
P830081Original Filing
S022 1988-07-07 Normal 180 Day Track
S021
S020
S019 1988-06-24 Normal 180 Day Track
S018 1988-03-28 Normal 180 Day Track
S017 1988-03-28 30-Day Supplement
S016 1988-01-20 30-Day Supplement
S015 1987-10-01 Normal 180 Day Track
S014 1987-07-01 Normal 180 Day Track
S013 1987-06-12 Normal 180 Day Track
S012 1987-03-19 Normal 180 Day Track
S011 1987-01-09 Normal 180 Day Track
S010 1986-12-09 Normal 180 Day Track
S009 1986-11-04 Normal 180 Day Track
S008 1986-10-20 Normal 180 Day Track
S007 1986-03-21
S006 1986-01-13
S005 1985-04-25
S004 1985-03-18 Normal 180 Day Track
S003 1985-02-27
S002 1985-01-24
S001 1984-12-07

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