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LEECO PRL-QUANT DIAGNOSTIC TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820039
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
15 days

LEECO PRL-QUANT DIAGNOSTIC TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820039
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
15 days