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LEECO T3% DIAGNOSTIC KIT

Page Type
Cleared 510(K)
510(k) Number
K822575
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1982
Days to Decision
36 days

LEECO T3% DIAGNOSTIC KIT

Page Type
Cleared 510(K)
510(k) Number
K822575
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1982
Days to Decision
36 days