The Food and Drug Administration's (FDA's) 510 (k) Process: A Systematic Review of 1000 Cases

P Shah, O Olavarria, N Dhanani, H Ciomperlik… - The American Journal of …, 2023 - Elsevier
Background The vast majority of devices cleared by the Food and Drug Administration (FDA)
are through the 510 (k) process, which allows medical devices to be quickly introduced into …
被引用次数：4 相关文章

The Food and Drug Administration's (FDA's) 510 (k) Process: A Systematic Review of 1000 Cases

P Shah, O Olavarria, N Dhanani… - The American Journal …, 2023 - amjmed.com
Background The vast majority of devices cleared by the Food and Drug Administration (FDA)
are through the 510 (k) process, which allows medical devices to be quickly introduced into …

The Food and Drug Administration's (FDA's) 510 (k) Process: A Systematic Review of 1000 Cases.

P Shah, O Olavarria, N Dhanani… - The American Journal …, 2022 - europepmc.org
Background The vast majority of devices cleared by the Food and Drug Administration (FDA)
are through the 510 (k) process which allows medical devices to be quickly introduced into …

The Food and Drug Administration's (FDA's) 510 (k) Process: A Systematic Review of 1000 Cases

P Shah, O Olavarria, N Dhanani… - … journal of medicine, 2023 - pubmed.ncbi.nlm.nih.gov
Background The vast majority of devices cleared by the Food and Drug Administration (FDA)
are through the 510 (k) process, which allows medical devices to be quickly introduced into …

The Food and Drug Administration's (FDA's) 510 (k) Process: A Systematic Review of 1000 Cases

P Shah, O Olavarria, N Dhanani, H Ciomperlik… - 2022 - scholarlycommons.hcahealthcare …
BACKGROUND: The vast majority of devices cleared by the Food and Drug Administration
(FDA) are through the 510 (k) process which allows medical devices to be quickly …