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IN VITRO DIAGNOSTIC STANDARDS

Page Type
Cleared 510(K)
510(k) Number
K802278
510(k) Type
Traditional
Applicant
SUPELCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1980
Days to Decision
73 days

IN VITRO DIAGNOSTIC STANDARDS

Page Type
Cleared 510(K)
510(k) Number
K802278
510(k) Type
Traditional
Applicant
SUPELCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1980
Days to Decision
73 days