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DIASCAN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K853553
510(k) Type
Traditional
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1985
Days to Decision
21 days

DIASCAN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K853553
510(k) Type
Traditional
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1985
Days to Decision
21 days