ClearanceBrief
510(k) K992471 ยท BSO Catheter, Conduction, Anesthetic

SIMS PORTEX EPIDURAL CATHETER, 20G MODEL# 4910-16/17; 21G MODEL# 4910-18

ApplicantSims Portex, Inc., Keene NH, US
DecisionSubstantially Equivalent, Oct 22, 1999
ReceivedJul 26, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992471

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.