Teleflex (TFX) Announces 510(k) Clearance and U.S. Launch of Spectre(TM) Guidewire

WAYNE, Pa.--(Healthcare Sales & Marketing Network)--Teleflex Incorporated (TFX), a leading global provider of medical technologies for critical care and surgery, has announced 510(k) clearance by the Food and Drug Administration and U.S. commercial launch ... Devices, Interventional, Cardiology, FDA, Product Launch Teleflex, Spectre Guidewire, percutaneous coronary intervention
Source: HSMN NewsFeed - Category: Pharmaceuticals Source Type: news