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2. Covidien Receives FDA 510(k) Clearance for Nellcor™ Pulse ...

   www.aol.com/2013/05/20/covidien-receives-fda-510...

   Covidien Receives FDA 510(k) Clearance for Nellcor™ Pulse Oximetry Motion Claims Nellcor pulse oximeters only FDA 510(k)-cleared oximeters compliant with ISO 80601-2-61 BOULDER, Colo.--(BUSINESS ...

3. Pulse oximetry - Wikipedia

   en.wikipedia.org/wiki/Pulse_oximetry

   A pulse oximeter probe applied to a person's finger. A pulse oximeter is a medical device that indirectly monitors the oxygen saturation of a patient's blood (as opposed to measuring oxygen saturation directly through a blood sample) and changes in blood volume in the skin, producing a photoplethysmogram that may be further processed into other measurements. [4]

4. Biox - Wikipedia

   en.wikipedia.org/wiki/Biox

   He led the team of pulse oximeter engineers which later developed the Ohmeda Biox 3700 [3] which was widely used in the anesthesia market in the mid-1980s. The first commercially available oximeters were produced by Hewlett-Packard, and were large, cumbersome, and expensive. These devices were of limited value because they were largely focused ...

5. Masimo's (MASI) Rad-G Pulse Oximeter Receives FDA Clearance - AOL

   www.aol.com/news/masimos-masi-rad-g-pulse...

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6. Masimo - Wikipedia

   en.wikipedia.org/wiki/Masimo

   In April 2023, the company received FDA approval for a pulse oximetry-based device for preventing opioid overdose by providing alerts of respiratory depression. The device—which was the subject of an innovation challenge issued by the FDA—received a De Novo classification allowing it to be distributed over-the-counter and through ...

7. FDA reviews evidence pulse oximeters less accurate on ... - AOL

   www.aol.com/news/fda-reviews-evidence-pulse...

   The Medical Devices Advisory Committee of the U.S. Food and Drug Administration (FDA) recently met to review the reported inaccuracy of pulse oximetry in patients with darker skin. The meeting ...