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LEECO LH-QUANT DIAGNOSTIC KIT

Page Type
Cleared 510(K)
510(k) Number
K810662
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1981
Days to Decision
20 days

LEECO LH-QUANT DIAGNOSTIC KIT

Page Type
Cleared 510(K)
510(k) Number
K810662
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1981
Days to Decision
20 days