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CHOLESTRAK HDL CHOLESTEROL HOME TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072836
510(k) Type
Traditional
Applicant
ACCUTECH, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2007
Days to Decision
85 days
Submission Type
Statement

CHOLESTRAK HDL CHOLESTEROL HOME TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072836
510(k) Type
Traditional
Applicant
ACCUTECH, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2007
Days to Decision
85 days
Submission Type
Statement