ClearanceBrief
510(k) K232230 ยท IOR Wheelchair, Mechanical

YJ-K1/K2 Wheelchair (YJ-K1F 16 NDE; YJ-K1F 16 NDS; YJ-K1F 18 NDE; YJ-K1F 18 NDS; YJ-K1F 20 NDE; YJ-K1F 20 NDS; YJ-K1F 18 NDEE; YJ-K1F 16 VDE; YJ-K1F 16 VDS; YJ-K1F 18 VDE; YJ-K1F 18 VDS; YJ-K1F 20 VDE; YJ-K1F 20 VDS; YJ-K2 16 VDFE; YJ-K2 16 VDFS; YJ-K2 18 VDFE; YJ-K2 18 VDFS; YJ-K2 20 VDFE; YJ-K2 20

ApplicantZhenjiang Assure Medical Equipment Co., Ltd., Zhenjiang City, CN
DecisionSubstantially Equivalent, Oct 3, 2023
ReceivedJul 27, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232230

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.