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LEECO TESTO-QUANT DIAG. KIT

Page Type
Cleared 510(K)
510(k) Number
K813059
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
17 days

LEECO TESTO-QUANT DIAG. KIT

Page Type
Cleared 510(K)
510(k) Number
K813059
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
17 days