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2. Expert Review of Medical Devices - Wikipedia

   en.wikipedia.org/wiki/Expert_Review_of_Medical...

   Expert Review of Medical Devices is a monthly peer-reviewed medical journal covering research on the clinical use of devices. It was established in 2004 and is published by Informa . According to the Journal Citation Reports , the journal has a 2013 impact factor of 1.784.

3. FDA warning letter - Wikipedia

   en.wikipedia.org/wiki/FDA_Warning_Letter

   The FDA considers a warning letter informal and advisory. It communicates the agency's position on a matter, but does not commit the FDA to an enforcement action. For that reason, the FDA does not consider a warning letter a final action on which it can be sued. [3]

4. Wireless device radiation and health - Wikipedia

   en.wikipedia.org/wiki/Wireless_device_radiation...

   The antennas contained in mobile phones, including smartphones, emit radiofrequency (RF) radiation (non-ionizing "radio waves" such as microwaves); the parts of the head or body nearest to the antenna can absorb this energy and convert it to heat or to synchronised molecular vibrations (the term 'heat', properly applies only to disordered molecular motion).

5. US FDA sends warning letter to Cardinal Health for marketing ...

   www.aol.com/news/us-fda-sends-warning-cardinal...

   The drug regulator during its inspection determined that Cardinal was an importer of two types of syringes sold under the Monoject brand. US FDA sends warning letter to Cardinal Health for ...

6. FDA Approves Abiomed's Impella Low Profile Sheath - AOL

   www.aol.com/news/fda-approves-abiomeds-impella...

   The FDA has granted 510(k) clearance to Abiomed Inc's (NASDAQ: ABMD) Impella Low Profile Sheath. Compared to the existing 14 French (Fr) sheath used for the placement of Impella CP, the new sheath ...

7. MiMedx reports US FDA warning letter for Axiofill, shares drop

   www.aol.com/news/mimedx-reports-us-fda-warning...

   Following a routine inspection this year, the FDA found Axiofill does not fall under Section 361 of the U.S. Public Health Service Act. MiMedx reports US FDA warning letter for Axiofill, shares ...

8. Boxed warning - Wikipedia

   en.wikipedia.org/wiki/Boxed_warning

   In the United States, a boxed warning (sometimes "black box warning", colloquially) is a type of warning that appears near the beginning of the package insert for certain prescription drugs, so called because the U.S. Food and Drug Administration specifies that it is formatted with a 'box' or border around the text [1] to emphasize its ...

9. Wireless Emergency Alerts - Wikipedia

   en.wikipedia.org/wiki/Wireless_Emergency_Alerts

   An example of a Wireless Emergency Alert on an Android smartphone, indicating a Tornado Warning in the covered area. Wireless Emergency Alerts (WEA), formerly known as the Commercial Mobile Alert System (CMAS) and, prior to that, as the Personal Localized Alerting Network (PLAN), [1] is an alerting network in the United States designed to disseminate emergency alerts to cell phones using Cell ...