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CORTISOL ENHANCED LUMINESCENCE ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K880687
510(k) Type
Traditional
Applicant
AMERSHAM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1988
Days to Decision
31 days

CORTISOL ENHANCED LUMINESCENCE ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K880687
510(k) Type
Traditional
Applicant
AMERSHAM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1988
Days to Decision
31 days