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DIATEK CANNON-CATHETER, MODEL CC5500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022662
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/9/2003
Days to Decision
273 days
Submission Type
Summary

DIATEK CANNON-CATHETER, MODEL CC5500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022662
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/9/2003
Days to Decision
273 days
Submission Type
Summary