ClearanceBrief
510(k) K912073 ยท LMC Camera, Multi Format, Radiological

POLAROID HELIOS LASER IMAGER

ApplicantPolaroid Medical Corp., Washington DC, US
DecisionSubstantially Equivalent, Aug 28, 1991
ReceivedMay 10, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912073

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.