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LEECO T3-QUANT DIAG. KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834348
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1984
Days to Decision
70 days

LEECO T3-QUANT DIAG. KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834348
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1984
Days to Decision
70 days