Last synced on 14 November 2025 at 11:06 pm

AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K131814
510(k) Type
Special
Applicant
AMECO MEDICAL INDUSTRIES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/26/2013
Days to Decision
36 days
Submission Type
Statement

AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K131814
510(k) Type
Special
Applicant
AMECO MEDICAL INDUSTRIES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/26/2013
Days to Decision
36 days
Submission Type
Statement