ClearanceBrief
510(k) K991023 ยท FRG Wrap, Sterilization

STERITITE PERFORATED BOTTOM RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02 - POLYPROPYLENE NON-WOVEN DISPOSABL

ApplicantCase Medical, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jan 27, 2000
ReceivedMar 29, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991023

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.