Medical Device Approvals Through the Premarket Approval Pathway in Obstetrics and Gynecology From 2000 to 2015: Process and Problems.
PMID : 27159747 · 2016
J, e, s, s, i, c, a, , R, , W, a, l, t, e, r, ;, , E, m, i, l, y, , H, a, y, m, a, n, ;, , S, h, e, l, u, n, , T, s, a, i, ;, , C, o, m, e, r, o, n, , W, , G, h, o, b, a, d, i, ;, , S, h, u, a, i, , X, u
Publicité
Résumé
Recent controversies surrounding obstetrics and gynecology devices, including a permanent sterilization device, pelvic meshes, and laparoscopic morcellators, highlight the need for deeper understanding of obstetrics and gynecology medical device regulation. The U.S. Food and Drug Administration premarket approval database was queried for approvals assigned to the obstetrics and gynecology advisory committee from January 2000 to December 2015. Eighteen device approvals occurred in the time period
Publicité
Source officielle
Voir sur PubMed →Données issues de PubMed / NCBI. Pour le texte intégral et les informations les plus récentes, consultez toujours la notice officielle.