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TANDEM VISUAL HCG IMMUNOENZYMETRIC

Page Type
Cleared 510(K)
510(k) Number
K834000
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1984
Days to Decision
74 days

TANDEM VISUAL HCG IMMUNOENZYMETRIC

Page Type
Cleared 510(K)
510(k) Number
K834000
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1984
Days to Decision
74 days