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The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C with BioGUARD Technology

Page Type
Cleared 510(K)
510(k) Number
K181563
510(k) Type
Traditional
Applicant
Access Scientific, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2018
Days to Decision
104 days
Submission Type
Summary

The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C with BioGUARD Technology

Page Type
Cleared 510(K)
510(k) Number
K181563
510(k) Type
Traditional
Applicant
Access Scientific, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2018
Days to Decision
104 days
Submission Type
Summary