ClearanceBrief
510(k) K830753 ยท LFL Instrument, Ultrasonic Surgical

NEEDLE GUIDE MODEL 21285A

ApplicantHewlett-Packard Co., Walker MI, US
DecisionSubstantially Equivalent, Jun 16, 1983
ReceivedMar 10, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830753

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.