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TANDEM HCG IMMUNOEZYMETRIC ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K821944
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1982
Days to Decision
23 days

TANDEM HCG IMMUNOEZYMETRIC ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K821944
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1982
Days to Decision
23 days