ClearanceBrief
510(k) K850785 ยท JXI Cuff, Nerve

FASTUBE NERVE REGENERATION DEVICE

ApplicantResearch Medical, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jul 10, 1985
ReceivedFeb 26, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850785

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.