ClearanceBrief
510(k) DEN220044 ยท QUU Simple In Vitro Diagnostic Device For The Detection Of Secreted Proteins From Bacillus Spp. In Human Clinical Samples

Active Anthrax DetectTM Plus Rapid Test

ApplicantInBios International, Inc., Seattle WA, US
DecisionUnknown, Feb 3, 2023
ReceivedJul 8, 2022
TypeDirect
FDA recordOpen on fda.gov

Recalls that name DEN220044

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.