LEX-WK-3MWNJQH8crawled 2022-07-22 13:40Z
FDA codifies requirements for the medical device De Novo classification process
Andrew Lu · Health Industry Washington Watch · Published October 14, 2021
Work details
- author
- Andrew Lu
- firm or organization
- Reed Smith LLP
- publication
- Health Industry Washington Watch
- practice area
- Administrative and Regulatory · Health Care and Life Sciences
- published
- 2021-10-14
Citation
Andrew Lu, FDA codifies requirements for the medical device De Novo classification process, Health Industry Washington Watch (October 14, 2021) [The Library at LexBlog, LEX-WK-3MWNJQH8, lexpid.org/3MWNJQH8]