ClearanceBrief
510(k) K921642 ยท LXH Orthopedic Manual Surgical Instrument

AMSEN DOUBLE-ENDED FORAMINAL PROBE

ApplicantAdvanced Med/Surg, Inc., Hayward CA, US
DecisionSubstantially Equivalent, Jun 3, 1992
ReceivedApr 6, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921642

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.