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DELFIA(TM) FERRITIN KIT

Page Type
Cleared 510(K)
510(k) Number
K872955
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1987
Days to Decision
23 days

DELFIA(TM) FERRITIN KIT

Page Type
Cleared 510(K)
510(k) Number
K872955
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1987
Days to Decision
23 days