ClearanceBrief
510(k) K081841 ยท ETY Tester, Auditory Impedance

AMPLIVOX OTOWAVE 102 HAND HELD PORTABLE TYMPANOMETER

ApplicantAmplivox, Ltd., Deer Field IL, US
DecisionSubstantially Equivalent, Jul 16, 2008
ReceivedJun 30, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081841

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.