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MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)

Page Type
Cleared 510(K)
510(k) Number
K940541
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1994
Days to Decision
273 days
Submission Type
Summary

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)

Page Type
Cleared 510(K)
510(k) Number
K940541
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1994
Days to Decision
273 days
Submission Type
Summary