ClearanceBrief
510(k) DEN220040 ยท QWO Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.

Fibresolve

ApplicantImvaria, Inc., Berkley CA, US
DecisionUnknown, Jan 12, 2024
ReceivedJun 29, 2022
TypeDirect
FDA recordOpen on fda.gov

Recalls that name DEN220040

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.