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DIAGNON FERRITIN 125 I RIA KIT

Page Type
Cleared 510(K)
510(k) Number
K830580
510(k) Type
Traditional
Applicant
IAGNON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1983
Days to Decision
71 days

DIAGNON FERRITIN 125 I RIA KIT

Page Type
Cleared 510(K)
510(k) Number
K830580
510(k) Type
Traditional
Applicant
IAGNON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1983
Days to Decision
71 days