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FERRITIN RIA KIT

Page Type
Cleared 510(K)
510(k) Number
K801580
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1980
Days to Decision
34 days

FERRITIN RIA KIT

Page Type
Cleared 510(K)
510(k) Number
K801580
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1980
Days to Decision
34 days