Lungpacer Medical begins subject enrolment in AeroNova system trial
Lungpacer Medical has commenced subject enrolment in its Phase II STimulation to Activate RespIration (STARI) trial, assessing the feasibility, effectiveness…
Lungpacer Medical has commenced subject enrolment in its Phase II STimulation to Activate RespIration (STARI) trial, assessing the feasibility, effectiveness…
Thermo Fisher Scientific has launched the new Molecular Microscope Diagnostic System for Lung (MMDx Lung), a new test to assist…
The US Food and Drug Administration (FDA) has granted 510(k) clearance to 4DMedical’s non-contrast, computed tomography (CT)-based ventilation-perfusion imaging technology,…
The US Food and Drug Administration (FDA) has granted approval for Thermo Fisher Scientific's Oncomine Dx Target Test as a…
The US Food and Drug Administration (FDA) has granted a second 510(k) clearance to expand the use of Respiree’s RS001…
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Neurent Medical's NEUROMARK system for the treatment of…
NeoGenomics has commercially launched the c-MET Companion Diagnostic (CDx) for use in non-small cell lung cancer (NSCLC), offering a 48-hour…
The US Food and Drug Administration (FDA) has granted breakthrough device designation to Roche's computational pathology companion diagnostic (CDx) VENTANA…
Novocure has obtained CE Mark approval for its Optune Lua device to treat adults with metastatic non-small cell lung cancer…
AccuStem Sciences is set to launch the microRNA Signature Classifier (MSC) blood test for the US lung cancer screening programmes.…