K233952 is an FDA 510(k) clearance for the DEKA ACE Pump System. This device is classified as a Alternate Controller Enabled Insulin Infusion Pump (Class II - Special Controls, product code QFG).
Submitted by Deka Research and Development (Manchester, US). The FDA issued a Cleared decision on March 13, 2024, 89 days after receiving the submission on December 15, 2023.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 880.5730. An Alternate Controller Enabled Insulin Infusion Pump (ace Insulin Pump) Is A Device Intended For The Infusion Of Insulin Into A Patient. The Ace Insulin Pump May Include Basal And Bolus Drug Delivery At Set Or Variable Rates. Ace Insulin Pumps Are Designed To Reliably And Securely Communicate With External Devices, Such As Automated Insulin Dosing Systems, To Allow Insulin Delivery Commands To Be Received, Executed, And Confirmed. Ace Insulin Pumps Are Intended To Be Used Both Alone And In Conjunction With Digitally Connected Medical Devices For The Purpose Of Insulin Delivery..