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DIAGNON FOLATE 125I RIA KIT

Page Type
Cleared 510(K)
510(k) Number
K841302
510(k) Type
Traditional
Applicant
DIAGNON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1984
Days to Decision
84 days

DIAGNON FOLATE 125I RIA KIT

Page Type
Cleared 510(K)
510(k) Number
K841302
510(k) Type
Traditional
Applicant
DIAGNON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1984
Days to Decision
84 days