Natus Manufacturing Limited
Natus Manufacturing Limited holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Natus Manufacturing Limited
FDA recalls by Natus Manufacturing Limited
- Z-1143-2021 — Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product Usage: indicated for draining cerebrospinal fluid (CFS) from the cerebral ventricles or the lumbar subarachnoid space as a means of reducing intracranial pressure and CSF volume when the insertion of a permanent, internal shunt is not indicated.
- Z-0951-2017 — Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and warm blankets and hospital linens; while, the Natus Warmette Dual Cabinet is designed to store and warm blankets and hospital linens in one compartment and fluids (irrigation and/or injection) in the other compartment within the storage times and warming temperatures recommended by the manufacturers of those items
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Natus Manufacturing Limited
- K242346 — Grass® MR Conditional/CT Cup Electrodes
- K173815 — Allergan Botox Needle Electrode
- K161430 — Myoject Luer Lock Needle Electrode
- K143433 — Dantec DCN Disposable Concentric Needle Electrodes-25mm, Dantec DCN Disposable Concentric Needle Electrodes-37mm, Dantec DCN Disposable Concentric Needle Electrodes-50mm, Dantec DCN Disposable Concentric Needle Electrodes-75mm
Data sourced from openFDA. This site is unofficial and independent of the FDA.