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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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