Teleflex lands FDA win for expanded claim on Arrow catheters
Teleflex (NYSE:TFX) won FDA clearance to market its Arrow peripherally inserted central catheter devices with Chlorag+ard antithrombogenic protection, which the company touts as the first of its kind.
ApniCure touts 510(k) clearance for Winx sleep therapy
Redwood City, Calif.-based ApniCure landed FDA 510(k) clearance for its Winx sleep therapy device, a mask-free system for patients with obstructive sleep apnea.
Nonin Medical wins 510(k) for expanded labeling on Onyx Vantage 9590 pulse oximeters
Nonin Medical announced expanded FDA clearance for its Onyx Vantage 9590 fingertip pulse oximeter, now allowing the device to be marketed for use on thumbs and toes.