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FIAX IGM TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K831608
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1983
Days to Decision
35 days

FIAX IGM TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K831608
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1983
Days to Decision
35 days