ClearanceBrief
510(k) K961392 ยท FJS Catheter, Peritoneal, Long-Term Indwelling

ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II

ApplicantSil-Med Corp., Taunton MA, US
DecisionSubstantially Equivalent, Jul 18, 1997
ReceivedApr 11, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961392

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.