ClearanceBrief
510(k) K932353 ยท IZL System, X-Ray, Mobile

HF-110A

ApplicantDynarad Corp., Deer Park NY, US
DecisionSubstantially Equivalent, Jan 31, 1994
ReceivedMay 13, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932353

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.