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ARKIVE (TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862085
510(k) Type
Traditional
Applicant
DIATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1987
Days to Decision
224 days

ARKIVE (TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862085
510(k) Type
Traditional
Applicant
DIATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1987
Days to Decision
224 days