Medical Device Network on MSN
Medtronic secures FDA clearance for MiniMed Go Smart MDI system
Medtronic has received US Food and Drug Administration (FDA) 510 (k) clearance for its MiniMed Go Smart MDI system, a ...
The FDA has granted 510(k) clearance to Medtronic for its MiniMed “Go Smart” multiple daily injection system — the first ...
Medtronic (NYSE:MDT) announced today that the FDA granted 510(k) clearance for its MiniMed Go app for multiple daily ...
The MiniMed Go™ system is cleared for individuals with insulin-requiring type 1 and type 2 diabetes aged 7 years and older, ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. The MiniMed 600 series insulin pumps include wireless ...
A real-world retrospective analysis published in Diabetes Care found that Medtronic’s MiniMed 780G insulin system users met American Diabetes Association time-in-range goals even on days when mealtime ...
Software Offers Therapy Considerations to Help Healthcare Professionals Make More Informed Treatment Decisions MINNEAPOLIS--(BUSINESS WIRE)-- Medtronic, Inc. today announced the Food and Drug ...
SILVER SPRING, Md., June 27, 2019 /PRNewswire/ -- The U.S. Food and Drug Administration is warning patients and health care providers that certain Medtronic MiniMed insulin pumps are being recalled ...
The technology was approved by FDA in June and unveiled at the Scientific Sessions of the American Diabetes Association. Medtronic today announced that its MiniMed Connect technology, which displays ...
Medtronic ($MDT) touted data from a retrospective study of 20,973 diabetes patients finding that the Threshold Suspend feature of its MiniMed 530G system is helpful ...
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