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LEECO E2 QUANT DIAG. TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K834586
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1984
Days to Decision
71 days

LEECO E2 QUANT DIAG. TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K834586
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1984
Days to Decision
71 days