ClearanceBrief
510(k) K081760 ยท IYE Accelerator, Linear, Medical

RSVP PHANTOM PELVIS, MODEL TLP260

ApplicantThe Phantom Laboratory, Inc., Salem NY, US
DecisionSubstantially Equivalent, Jul 29, 2008
ReceivedJun 20, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081760

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.