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IGE-QUANT DIAGNOSTIC TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K831208
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1983
Days to Decision
25 days

IGE-QUANT DIAGNOSTIC TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K831208
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1983
Days to Decision
25 days