Last synced on 14 November 2025 at 11:06 pm

THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN

Page Type
Cleared 510(K)
510(k) Number
K131023
510(k) Type
Traditional
Applicant
Medical Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
182 days
Submission Type
Statement

THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN

Page Type
Cleared 510(K)
510(k) Number
K131023
510(k) Type
Traditional
Applicant
Medical Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
182 days
Submission Type
Statement