ClearanceBrief
510(k) K910441 ยท DPT Probe, Blood-Flow, Extravascular

FLOSCOPE MICRODOP

ApplicantAdvance Medical Device, Inc., Berlin NJ, US
DecisionSubstantially Equivalent, Mar 21, 1991
ReceivedJan 31, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910441

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.