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ACUTE AND CHRONIC CATHETER REPAIR KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092797
510(k) Type
Traditional
Applicant
KENDALL
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
11/19/2009
Days to Decision
69 days
Submission Type
Summary

ACUTE AND CHRONIC CATHETER REPAIR KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092797
510(k) Type
Traditional
Applicant
KENDALL
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
11/19/2009
Days to Decision
69 days
Submission Type
Summary