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SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE

Page Type
Cleared 510(K)
510(k) Number
K935694
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
98 days
Submission Type
Summary

SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE

Page Type
Cleared 510(K)
510(k) Number
K935694
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
98 days
Submission Type
Summary