ClearanceBrief
510(k) K222305 · LCX Kit, Test, Pregnancy, Hcg, Over The Counter

MissLan™ Digital Pregnancy Rapid Test

ApplicantGuangzhou Decheng Biotechnology Co., Ltd., Guangzhou, CN
DecisionSubstantially Equivalent, Nov 30, 2022
ReceivedAug 1, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222305

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.