ClearanceBrief
510(k) K950914 ยท HLJ Ophthalmoscope, Battery-Powered

RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER ANAESTHETIC MODEL 2,5 V/220 V OR 110 C 3,5 V/V

ApplicantRudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE
DecisionSubstantially Equivalent, Jul 24, 1995
ReceivedFeb 23, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950914

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.