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FDA 510(k) Applications Submitted by SpectraWAVE Inc
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230691
03/13/2023
HyperVueÖ Imaging System
SpectraWAVE Inc
K221257
05/02/2022
SpectraWAVE Imaging System
SpectraWAVE Inc
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