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PHASE II FSH KIT

Page Type
Cleared 510(K)
510(k) Number
K883279
510(k) Type
Traditional
Applicant
VITEK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1988
Days to Decision
37 days

PHASE II FSH KIT

Page Type
Cleared 510(K)
510(k) Number
K883279
510(k) Type
Traditional
Applicant
VITEK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1988
Days to Decision
37 days