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  2. FDA-authorized Powecom KN95 masks are in stock at Amazon - AOL

    www.aol.com/news/kn95-masks-amazon-powecom...

    Powecom is one of the only KN95 mask brands authorized by the FDA.

  3. Stock up on KN95s: These FDA-authorized masks are just ... - AOL

    www.aol.com/lifestyle/stock-kn95s-fda-authorized...

    In fact, during the early days of the pandemic when medical-grade masks were in particularly short supply, the FDA granted what’s known as ‘emergency use authorization’ (EUA) for KN95 masks ...

  4. FDA Center for Devices and Radiological Health - Wikipedia

    en.wikipedia.org/wiki/FDA_Center_for_Devices_and...

    Examples of products that CDRH regulates include medical devices ranging from tongue depressors and personal protective equipment (PPE) to pacemakers and robotic surgical systems, and medical and non-medical radiation-emitting electronic products such as lasers, x-ray systems, ultrasound equipment, microwave ovens, and color televisions.

  5. Pulsed electromagnetic field therapy - Wikipedia

    en.wikipedia.org/wiki/Pulsed_electromagnetic...

    In 2004, a pulsed electromagnetic field system was approved by the FDA as an adjunct to cervical fusion surgery in patients at high risk for non-fusion. [6] On 8/9 September 2020 the FDA recommended to shift PEMF medical devices from the Class 3 category to a Class 2 status. [7]

  6. Stock up on KN95s after the updated CDC guidelines: These FDA ...

    www.aol.com/lifestyle/stock-kn95s-updated-cdc...

    Stock up on KN95s after the updated CDC guidelines: These FDA-approved masks are on sale for $1.50 a pop at Amazon Devon Kelley,Izabella Zaydenberg October 30, 2021 at 9:13 AM

  7. Home medical equipment - Wikipedia

    en.wikipedia.org/wiki/Home_medical_equipment

    Home medical equipment is a category of devices used for patients whose care is being managed from a home or other private facility managed by a nonprofessional caregiver or family member. It is often referred to as "durable" medical equipment (DME) as it is intended to withstand repeated use by non-professionals or the patient, and is ...

  8. Medical Device Regulation Act - Wikipedia

    en.wikipedia.org/wiki/Medical_Device_Regulation_Act

    Medical device is to be for use in supporting or sustaining human life, of substantial importance in preventing impairment of human health, or presents a potential unreasonable risk of illness or injury, is to be subject, premarket approval to provide reasonable assurance of its safety and effectiveness. Classification Panels for Medical Devices

  9. Validation and verification (medical devices) - Wikipedia

    en.wikipedia.org/wiki/Validation_and...

    For instance, a regulatory agency (such as CE or FDA) may ensure that a product has been validated for general use before approval. An individual laboratory that introduces such an approved medical device may then not need to perform their own validation, but generally still need to perform verification to ensure that the device works correctly ...

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