ClearanceBrief
510(k) K970340 ยท LZI Device, Assistive Listening

AIR CONDUCTION ASSISTIVE LISTENING DEVICE.PERSONAL AMPLIFIER

ApplicantBellab, Gothenburg, SE
DecisionSubstantially Equivalent, Mar 26, 1997
ReceivedJan 29, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970340

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.