ClearanceBrief
510(k) K970969 ยท KOB Catheter, Suprapubic (And Accessories)

KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET

ApplicantThe Kendal Co., Mansfield MA, US
DecisionSubstantially Equivalent, Apr 23, 1997
ReceivedMar 17, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970969

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.