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AMERICAN CATHETER, MODEL W3

Page Type
Cleared 510(K)
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)
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