Medline Industries, LP - FDA 510(k) Cleared Devices
Recent clearances: Hudson RCI® Infant Dri-TechTM Breathing Circuits (HUD99060 / Dri-Tech with 78” Infant Circuit, HUD99060KIT / Dri-Tech with 78” Infant Circuit Kit, HUD99001KIT / Single Limb Infant Circuit Dri-Tech Kit, HUD99009KIT / Dri-Tech with 60” Infant Circuit Kit, HUD99018KIT / Dri-Tech with 44” Infant Circuit Kit, HUD870NKIT / Dri-Tech Infant Accessory Bag, HUD1631 / Infant Wye Connector with Swivel), Konig Bell Circumcision Clamp, Namic Radial Arm Band, 23 cm (DYNJRADBAND)
29
Total
29
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medline Industries, LP Anesthesiology ✕
7 devices
Cleared
Mar 25, 2026
Hudson RCI® Infant Dri-TechTM Breathing Circuits (HUD99060 / Dri-Tech with...
Anesthesiology
176d
Cleared
Jul 02, 2025
Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant
Anesthesiology
149d
Cleared
Dec 19, 2024
Hudson RCI Comfort Flo® CubCannula™
Anesthesiology
182d
Cleared
Sep 27, 2024
Hudson RCI® Comfort Flo Nasal Cannula
Anesthesiology
249d
Cleared
Jun 04, 2024
Hudson RCI Dri-Tech Breathing Circuits
Anesthesiology
167d
Cleared
Jan 04, 2024
Hudson RCI® AddiPak® Unit Dose Vial
Anesthesiology
266d
Cleared
Oct 31, 2023
Hudson RCI® TurboMist™ Nebulizer System
Anesthesiology
242d