Last synced on 18 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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