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12F Tri-Flow Triple Lumen Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181175
510(k) Type
Traditional
Applicant
Medical Components Inc. (Dba Medcomp)
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/5/2018
Days to Decision
64 days
Submission Type
Summary

12F Tri-Flow Triple Lumen Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181175
510(k) Type
Traditional
Applicant
Medical Components Inc. (Dba Medcomp)
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/5/2018
Days to Decision
64 days
Submission Type
Summary