Last synced on 25 January 2026 at 3:41 am

SIEMENS MULTIVIEW WORKSTATION ENHANCED WITH DIAGNOSTIC STATEMENTS (REST ECG)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980625
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1998
Days to Decision
90 days
Submission Type
Summary

SIEMENS MULTIVIEW WORKSTATION ENHANCED WITH DIAGNOSTIC STATEMENTS (REST ECG)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980625
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1998
Days to Decision
90 days
Submission Type
Summary