ClearanceBrief
510(k) K983802 ยท MJN Catheter, Intravascular Occluding, Temporary

LMI CAROTID ENDARTERECTOMY SHUNT CATHETER, MODEL #'S CES, CESR, CESB, CESRB, CEST, CESTR, CESTB, CESTRB, CES-SB, CESR-SB

ApplicantLucas Medical, Inc., Anaheim CA, US
DecisionSubstantially Equivalent, Jul 30, 1999
ReceivedOct 28, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983802

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.