ClearanceBrief
510(k) K921319 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30

ApplicantNeuromed, Inc., Ft. Lauderdale FL, US
DecisionSubstantially Equivalent, May 5, 1993
ReceivedMar 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921319

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.