ClearanceBrief
510(k) K242209 ยท PTC Uric Acid Test System For At Home Prescription Use

UASure II Blood Uric Acid Monitoring System

ApplicantApex BioTechnology Corp., Hsinchu, TW
DecisionSubstantially Equivalent, Apr 4, 2025
ReceivedJul 29, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242209

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.