FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SmartGuard technology; Predictive Low Glucose technology

K Number: K251217 · Decision Aug 29, 2025
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
19
Applicant Total
8
Review Days
130

Basic Information

Device Name
SmartGuard technology; Predictive Low Glucose technology
K Number
K251217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1356
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Minimed, Inc.
Date Received
April 21, 2025
Decision Date
August 29, 2025
Product Code
QJI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QJI Interoperable Automated Glycemic Controller

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QJI), ordered by most recent decision date.

View all

Other Clearances by Medtronic Minimed, Inc.

K Number Device Name
K253743 MiniMed Flex pump
K253470 MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)
K253585 SmartGuard technology; Predictive Low Glucose technology
K251032 MiniMed 780G insulin pump
K210714 Extended Reservoir
K151236 MiniMed Connect kit, MiniMed Connect uploader, MiniMed Connect app, CareLink Connect (CareLink Personal)
K070438 MEDTRONIC MINIMED CARELINK USB CONNECTOR, MODEL NMT 7305