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

Omnipod GO Insulin Delivery Device

K Number: K223372 · Decision Apr 24, 2023
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
83
Applicant Total
23
Review Days
171

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Basic Information

Device Name
Omnipod GO Insulin Delivery Device
K Number
K223372
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Insulet Corporation
Date Received
November 4, 2022
Decision Date
April 24, 2023
Product Code
LZG
Advisory Committee
General Hospital
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
LZG Pump, Infusion, Insulin

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Other Clearances by Insulet Corporation

K Number Device Name
K251779 Omnipod 5 algorithm
K241777 SmartAdjust™ Technology
K232741 SmartAdjust(TM) technology
K231826 Omnipod 5 ACE Pump
K231824 SmartBolus Calculator
K220394 SmartAdjust(TM) technology
K222239 SmartBolus Calculator
K203772 Omnipod 5 SmartBolus Calculator
K203768 Omnipod 5 ACE Pump (Pod)
K203774 SmartAdjust technology
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