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CARDIOFOCAL COLLIMATOR

Page Type
Cleared 510(K)
510(k) Number
K914179
510(k) Type
Traditional
Applicant
SIEMENS GAMMASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1991
Days to Decision
42 days
Submission Type
Statement

CARDIOFOCAL COLLIMATOR

Page Type
Cleared 510(K)
510(k) Number
K914179
510(k) Type
Traditional
Applicant
SIEMENS GAMMASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1991
Days to Decision
42 days
Submission Type
Statement