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MEDILOG 6000-FD REPORT GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K890330
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1989
Days to Decision
87 days

MEDILOG 6000-FD REPORT GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K890330
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1989
Days to Decision
87 days