ClearanceBrief
510(k) DEN200001 ยท QMA Blood Collection Device For Cell-Free Nucleic Acid

Cell-Free DNA BCT

ApplicantStreck, Inc., La Vista NE, US
DecisionUnknown, Aug 7, 2020
ReceivedJan 10, 2020
TypeDirect
FDA recordOpen on fda.gov

Recalls that name DEN200001

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.