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ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT

Page Type
Cleared 510(K)
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)
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