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FLUOROVISION CONTRAST ENHANCER

Page Type
Cleared 510(K)
510(k) Number
K864584
510(k) Type
Traditional
Applicant
DIGIVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1986
Days to Decision
39 days

FLUOROVISION CONTRAST ENHANCER

Page Type
Cleared 510(K)
510(k) Number
K864584
510(k) Type
Traditional
Applicant
DIGIVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1986
Days to Decision
39 days