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ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071998
510(k) Type
Special
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2007
Days to Decision
65 days
Submission Type
Summary

ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071998
510(k) Type
Special
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2007
Days to Decision
65 days
Submission Type
Summary