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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact