ClearanceBrief
510(k) K233001 ยท ETN Stimulator, Nerve

Bioscope Neuromonitor Device

ApplicantBiosys Biyomedikal Muhendislik San. VE Tic. A.S., Ankara, TR
DecisionSubstantially Equivalent, Dec 13, 2024
ReceivedSep 22, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233001

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.