FDA 483 - Bard Access Systems, Inc. (BAS) - August 21, 1993

This document is an exhibit related to a 510(k) submission (K924250) for the Bard Plastic Low Profile Subcutaneous Port. It details the regulatory status and certification statements for various kit components, including a winged infusion set, vein pick, and disposable syringe. Bard Access Systems, Inc. provides information on how these components are purchased and processed, noting that certifications are based on supplier verifications.