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KYOKKO UM SERIES INTENSIFYING SCREEN

Page Type
Cleared 510(K)
510(k) Number
K942399
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1994
Days to Decision
22 days
Submission Type
Summary

KYOKKO UM SERIES INTENSIFYING SCREEN

Page Type
Cleared 510(K)
510(k) Number
K942399
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1994
Days to Decision
22 days
Submission Type
Summary