Last synced on 30 May 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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