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14 FR TWO-LUMEN HEMODIALYSIS CATHERIZATION KIT WITH BLUE FLEXTIP ARROWG+ARD BLUE CATHETER FOR HIGH VOLUME INFUSIONS, PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993933
510(k) Type
Traditional
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2000
Days to Decision
301 days
Submission Type
Summary

14 FR TWO-LUMEN HEMODIALYSIS CATHERIZATION KIT WITH BLUE FLEXTIP ARROWG+ARD BLUE CATHETER FOR HIGH VOLUME INFUSIONS, PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993933
510(k) Type
Traditional
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2000
Days to Decision
301 days
Submission Type
Summary