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AMECATH DUAL LUMEN HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K123943
510(k) Type
Traditional
Applicant
Ameco Medical Industries
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2013
Days to Decision
103 days
Submission Type
Statement

AMECATH DUAL LUMEN HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K123943
510(k) Type
Traditional
Applicant
Ameco Medical Industries
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2013
Days to Decision
103 days
Submission Type
Statement