Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

PubMed

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

RevistaObstetrics and gynecology
Año2016
PMID27159747

Resumen

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

Fuente oficial

Ver en PubMed →

Datos obtenidos de PubMed / NCBI. Para consultar el texto completo y la información más reciente, remítase siempre al registro oficial.

↑