ClearanceBrief
510(k) K192278 ยท HIH Hysteroscope (And Accessories)

Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable Sheath (Diagnostic)

ApplicantUvision360, Inc., Raleigh NC, US
DecisionSubstantially Equivalent, Nov 1, 2019
ReceivedAug 22, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K192278

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.