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SIEMEN'S SIREMOBILE II C-ARM

Page Type
Cleared 510(K)
510(k) Number
K902983
510(k) Type
Traditional
Applicant
ELECTROMEK DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1990
Days to Decision
133 days

SIEMEN'S SIREMOBILE II C-ARM

Page Type
Cleared 510(K)
510(k) Number
K902983
510(k) Type
Traditional
Applicant
ELECTROMEK DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1990
Days to Decision
133 days