ClearanceBrief
510(k) K895500 ยท IYE Accelerator, Linear, Medical

PATIENT POSITIONING ACCESSORIES

ApplicantPerkins Mfg. Co., Dallas TX, US
DecisionSubstantially Equivalent, Nov 6, 1989
ReceivedSep 12, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895500

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.