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  2. Medical device reporting - Wikipedia

    en.wikipedia.org/wiki/Medical_device_reporting

    The device user facility reporting section of SMDA became effective on November 28, 1991. To implement SMDA, FDA published a tentative final rule in the Federal Register on November 26, 1991, inviting comments; over 300 comments were received. On June 16, 1992, the President signed into law the Medical Devices Amendments of 1992 (Public Law 102 ...

  3. FDA Center for Devices and Radiological Health - Wikipedia

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

    The FD&C allowed the FDA to perform factory inspections and prohibited misbranded marketing of cosmetic and therapeutic medical devices. [10] In the 1970s, Congress responded to the public's desire for additional oversight over medical devices by passing the Medical Device Amendments of 1976 (MDA) to the FD&C.

  4. List of high schools in New Jersey - Wikipedia

    en.wikipedia.org/wiki/List_of_high_schools_in...

    This is a list of high schools, including those open and closed, in the U.S. state of New Jersey. This list is incomplete ; you can help by adding missing items . ( August 2008 )

  5. Safe Medical Device Amendments of 1990 - Wikipedia

    en.wikipedia.org/wiki/Safe_Medical_Device...

    Safe Medical Device Amendments of 1990; Long title: An Act to amend the Federal Food, Drug, and Cosmetic Act to make improvements in the regulation of medical devices, and for other purposes. Enacted by: the 101st United States Congress: Effective: November 28, 1990: Citations; Public law: 101-629: Statutes at Large: 104 Stat. 4511 ...

  6. Title 21 of the Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Title_21_of_the_Code_of...

    The 800 series are for medical devices: 803 Medical device reporting; 814 Premarket approval of medical devices [3] 820 et seq. Quality system regulations (analogous to cGMP, but structured like ISO) [4] 860 et seq. Listing of specific approved devices and how they are classified; The 900 series covers mammography quality requirements enforced ...

  7. MedWatch - Wikipedia

    en.wikipedia.org/wiki/MedWatch

    Voluntary reporting by healthcare professionals, consumers, and patients is conducted on a single, one-page reporting form (Form FDA 3500 [2]). Reporting can be conducted online, [3] by phone, or by submitting the MedWatch 3500 form by mail or fax. In 2013, MedWatch introduced Form 3500B, which is designed to facilitate reporting by healthcare ...

  8. List of school districts in New Jersey - Wikipedia

    en.wikipedia.org/wiki/List_of_school_districts...

    Northvale Public Schools – K-8; Norwood Public School District – K-8; Oakland Public Schools – K-8; Old Tappan Public Schools – K-8; Oradell Public School District – K-6; Palisades Park Public School District – PreK-12; Paramus Public Schools – PreK-12; Park Ridge Public Schools – PreK-12; Pascack Valley Regional High School ...

  9. Food and Drug Administration Amendments Act of 2007

    en.wikipedia.org/wiki/Food_and_Drug...

    It requires the FDA to submit an annual report to congressional committees that includes: (1) the number of devices approved in the preceding year for which there is a pediatric subpopulation that suffers from the disease; (2) the number of approved devices labeled for use in pediatric patients; (3) the number of fee-exempt devices approved ...