ClearanceBrief
510(k) K802750 ยท KLW Masker, Tinnitus

NUVOX BEDSIDE TINNITUS MASKER

ApplicantHal-Hen Co., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 31, 1980
ReceivedNov 4, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802750

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.