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BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013634
510(k) Type
Traditional
Applicant
BIOTEQUE CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/9/2002
Days to Decision
246 days
Submission Type
Summary

BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013634
510(k) Type
Traditional
Applicant
BIOTEQUE CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/9/2002
Days to Decision
246 days
Submission Type
Summary