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POURCHEZ RETRO TWIN LUMEN CHRONIC HEMODIALYSIS CATHETER WITH SEPARATED TIPS (WITH AND WITHOUT SIDE HOLES)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022000
510(k) Type
Special
Applicant
Spire Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2002
Days to Decision
30 days
Submission Type
Summary

POURCHEZ RETRO TWIN LUMEN CHRONIC HEMODIALYSIS CATHETER WITH SEPARATED TIPS (WITH AND WITHOUT SIDE HOLES)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022000
510(k) Type
Special
Applicant
Spire Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2002
Days to Decision
30 days
Submission Type
Summary