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FERRITIN KIT

Page Type
Cleared 510(K)
510(k) Number
K812597
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1981
Days to Decision
35 days

FERRITIN KIT

Page Type
Cleared 510(K)
510(k) Number
K812597
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1981
Days to Decision
35 days