FDA 510(k) Applications Submitted by Allison London Brown

FDA 510(k) Number Submission Date Device Name Applicant
K210512 02/23/2021 LUMINELLE DTx System Uvision360, Inc.
K190827 04/01/2019 Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable Sheath Rigid UVision360 Inc.
K181909 07/17/2018 Luminelle DTx Hysteroscopy System UVision360 Inc.
K192278 08/22/2019 Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable Sheath (Diagnostic) UVision360 Inc.


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