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LITEBOX DIAGNOSTIC REVIEW WORKSTATION

Page Type
Cleared 510(K)
510(k) Number
K901158
510(k) Type
Traditional
Applicant
SIEMENS GAMMASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1990
Days to Decision
37 days

LITEBOX DIAGNOSTIC REVIEW WORKSTATION

Page Type
Cleared 510(K)
510(k) Number
K901158
510(k) Type
Traditional
Applicant
SIEMENS GAMMASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1990
Days to Decision
37 days