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ARROW ECHOGENIC INTRODUCER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K040100
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2004
Days to Decision
41 days
Submission Type
Summary

ARROW ECHOGENIC INTRODUCER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K040100
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2004
Days to Decision
41 days
Submission Type
Summary