ClearanceBrief
510(k) K890445 ยท LXI Guide, Drill, Ligament

PERSONAL ALERT ASSIST DEVICE

ApplicantSilent Call Corp., Clarkston MI, US
DecisionSubstantially Equivalent, May 19, 1989
ReceivedJan 27, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890445

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.