ClearanceBrief
510(k) K932131 ยท EQH Source, Carrier, Fiberoptic Light

MID LABS TWIN ILLUMINATOR

ApplicantMedical Instrument Development Laboratories, Inc., San Leandro CA, US
DecisionSubstantially Equivalent, Apr 1, 1994
ReceivedMay 3, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932131

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.