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

InPen System App (MMT-8060 (iOS), MMT-8061 (Android))

K Number: K242775 · Decision Nov 12, 2024
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
54
Applicant Total
48
Review Days
60

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Basic Information

Device Name
InPen System App (MMT-8060 (iOS), MMT-8061 (Android))
K Number
K242775
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1890
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Minimed
Date Received
September 13, 2024
Decision Date
November 12, 2024
Product Code
NDC
Advisory Committee
Anesthesiology
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
NDC Calculator, Drug Dose

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Other Clearances by Medtronic Minimed

K Number Device Name
K253701 SmartGuard Technology; Predictive Low Glucose Technology
K253512 MiniMed Go App
K241622 Extended Reservoir; MiniMed Reservoir
K160860 MiniMed Quick-serter
K120206 MEDTRONIC MINIMED PARADIGM INSULIN PUMPS
K100432 POLYFIN INFUSION SET, MODELS MMT-165, MMT-365, MMT-366, MMT-312S AND MMT-312L AND SOF-SET INFUSION SETS
K073356 PARADIGM INSULIN INFUSION PUMP, MODELS MMT-512, MMT-712, MMT-515 AND MMT-715
K053177 MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712E
K052431 MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1
K052432 MEDTRONIC MINIMED PARADIGM LEAPFROG II INFUSION SET, MODELS MMT-802S1, MMT-802L1, MMT-802S2, MMT-802L2
Search all 48 clearances from Medtronic Minimed →