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MAGNETOM P8 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K911991
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1991
Days to Decision
74 days
Submission Type
Summary

MAGNETOM P8 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K911991
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1991
Days to Decision
74 days
Submission Type
Summary