ClearanceBrief
510(k) K220035 ยท HDX Dilator, Vaginal

Milli Vaginal Dilator

ApplicantMaterna Medical, Mountain View CA, US
DecisionSubstantially Equivalent, Feb 27, 2023
ReceivedJan 5, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220035

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.