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Ndd Medizintechnik AG
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K230178
EasyOne Sky Spirometer
October 19, 2023
K221250
EasyOne Filter
November 22, 2022
K161534
EasyOne Pro Respiratory Analysis System
February 22, 2017
K161536
EasyOne Air Spirometer
January 5, 2017