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MAG RESON DIAG DEV ACCESS SPEC PURP REC ONLY COIL

Page Type
Cleared 510(K)
510(k) Number
K901952
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
108 days

MAG RESON DIAG DEV ACCESS SPEC PURP REC ONLY COIL

Page Type
Cleared 510(K)
510(k) Number
K901952
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
108 days