The Visby Medical Women's Sexual Health Test received marketing authorization to diagnose chlamydia, gonorrhea, and trichomoniasis in women.
Withings . Withings has announced its BPM Vision blood pressure monitor will be available in the U.S. from April 2, having cleared the Food and Drug Administration (FDA)’s strin ...
Bright Uro announced today that it has received FDA 510(k) clearance for its Glean urodynamic analyzer system.
Resuscitation equipment, pediatric forms of medicine and the addition of pulse oximeters are a few examples of a broader ...
MyChesCo on MSN9h
Teleflex Secures FDA Clearance for AC3 Range IABP, Enhancing Cardiac Patient TransportTeleflex Incorporated (NYSE: TFX) has announced that its AC3 Range™ Intra-Aortic Balloon Pump (IABP) has received FDA 510(k) ...
The FDA has approved Gvoke VialDx (glucagon) for IV use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the GI tract.
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