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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