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19 GA PLASTIC REINFORCED EPIDURAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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