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19 GA PLASTIC REINFORCED EPIDURAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K001587
510(k) Type
Special
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2000
Days to Decision
50 days
Submission Type
Summary

19 GA PLASTIC REINFORCED EPIDURAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K001587
510(k) Type
Special
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2000
Days to Decision
50 days
Submission Type
Summary