ClearanceBrief
510(k) K872441 ยท DPT Probe, Blood-Flow, Extravascular

HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR

ApplicantAdvanced Technology Laboratories, Inc., Bothell WA, US
DecisionSubstantially Equivalent, Feb 19, 1988
ReceivedJun 19, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872441

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.