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SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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