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QUIKREAD(R) WHOLE BLOOD TRIGLYCERIDE TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K897169
510(k) Type
Traditional
Applicant
PHOTEC DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1990
Days to Decision
57 days

QUIKREAD(R) WHOLE BLOOD TRIGLYCERIDE TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K897169
510(k) Type
Traditional
Applicant
PHOTEC DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1990
Days to Decision
57 days