ClearanceBrief
510(k) K963570 ยท FMJ Manometer, Spinal-Fluid

SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)

ApplicantSmiths Industries Medical Systems, Inc., Keene NH, US
DecisionSubstantially Equivalent, Oct 18, 1996
ReceivedSep 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963570

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.