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AMERICAN CATHETER, MODEL W3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030538
510(k) Type
Traditional
Applicant
CATHETER LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2003
Days to Decision
18 days
Submission Type
Summary

AMERICAN CATHETER, MODEL W3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030538
510(k) Type
Traditional
Applicant
CATHETER LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2003
Days to Decision
18 days
Submission Type
Summary