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IN VITRO DIAGNOSTIC RADIOIMMUNOASSAY

Page Type
Cleared 510(K)
510(k) Number
K813525
510(k) Type
Traditional
Applicant
MICROMEDIC SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/31/1981
Days to Decision
15 days

IN VITRO DIAGNOSTIC RADIOIMMUNOASSAY

Page Type
Cleared 510(K)
510(k) Number
K813525
510(k) Type
Traditional
Applicant
MICROMEDIC SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/31/1981
Days to Decision
15 days