FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

SmartPilot YpsoMate NS-A2.25

K Number: K243901 · Decision Aug 28, 2025
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
6
Applicant Total
12
Review Days
252

Basic Information

Device Name
SmartPilot YpsoMate NS-A2.25
K Number
K243901
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ypsomed AG
Date Received
December 19, 2024
Decision Date
August 28, 2025
Product Code
QOG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
QOG Injection Data Capture Device

Similar 510(k) Clearances

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

View all

Other Clearances by Ypsomed AG

K Number Device Name
K171984 Clickfine Pen Needle, Penfine Classic Pen Needle
K163400 Orbit Inserter
K150921 Orbit Infusion Set
K152514 Clickfine AutoProtect Pen Needle
K150662 Clickfine Pen Needle, Penfine Classic Pen Needle (other trade names anticipated)
K131125 CLICKFINE PEN NEEDLE
K131123 CLICKFINE AUTOPROTECT PEN NEEDLE
K130468 ORBIT INFUSION SET
K110312 CLICKFINE AUTOPROTECT PEN NEEDLE
K102108 CLICKFINE PEN NEEDLE
Search all 12 clearances from Ypsomed AG →