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FDA 510(k) Applications Submitted by Vitalograph Ireland Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200550
03/03/2020
Vitalograph Model 2120 In2itive eDiary
Vitalograph Ireland Ltd.
K221030
04/07/2022
Model 9100 PFT/DICO
Vitalograph Ireland Ltd.
K201562
06/10/2020
Spirotrac
Vitalograph Ireland Ltd.
K212938
09/15/2021
Vitalograph Model 6000 Alpha
Vitalograph Ireland Ltd.
K223818
12/21/2022
Model 9160 VitaloQUB
Vitalograph Ireland Ltd.
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