FDA 510(k) Applications Submitted by Phyllis Kondor

FDA 510(k) Number	Submission Date	Device Name	Applicant
K231058	04/13/2023	Hudson RCI« AddiPak« Unit Dose Vial	Medline Industries, LP
K234032	12/20/2023	Hudson RCI Dri-Tech Breathing Circuits; HUD99035/Dri-Tech Adult Circuit; HUD99035KIT/Dri-Tech Adult Circuit Kit; HUD99098KIT/Single Limb Adult Dri-Tech Kit; HUD99098KITF/Single Limb Adult Dri-Tech Filter Kit; HUD900/Dri-Tech Ventilator Accessory; HUD901/D	Medline Industries, LP