FDA 510(k) Applications Submitted by Alpha Omega Engineering Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K220553 02/28/2022 Neuro Omega System, NeuroSmart System Alpha Omega Engineering Ltd.
K123796 12/10/2012 NEURO OMEGA SYSTEM ALPHA OMEGA ENGINEERING LTD.
K191739 06/28/2019 Sterile LeadConfirm Alpha Omega Engineering Ltd.
K172042 07/06/2017 NeuroNav System, NeuroSmart System Alpha Omega Engineering Ltd.


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