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PALINDROME P HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092205
510(k) Type
Traditional
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/30/2009
Days to Decision
100 days
Submission Type
Summary

PALINDROME P HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092205
510(k) Type
Traditional
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/30/2009
Days to Decision
100 days
Submission Type
Summary