Medical Devices; General and Plastic Surgery Devices; Classification of the Electrosurgical Device for Over-the-Counter Aesthetic Use. Final order.
【연구 목적】 미국 식품의약국(FDA)은 일반 의약품 및 성형외과 기구 범주에서 가정용 미용 목적으로 판매되는 전기소작기(electrosurgical device)를 특수 통제(special controls)가 적용되는 Class II 기기로 분류하는 최종 명령을 내렸다.
APA
(2016). Medical Devices; General and Plastic Surgery Devices; Classification of the Electrosurgical Device for Over-the-Counter Aesthetic Use. Final order.. Federal register, 81(125), 42243-5.
MLA
. "Medical Devices; General and Plastic Surgery Devices; Classification of the Electrosurgical Device for Over-the-Counter Aesthetic Use. Final order.." Federal register, vol. 81, no. 125, 2016, pp. 42243-5.
PMID
27373015
Abstract
The Food and Drug Administration (FDA) is classifying the electrosurgical device for over-the-counter aesthetic use into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the electrosurgical device for over-the-counter aesthetic use's classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 기타 | class II
|
scispacy | 1 |
MeSH Terms
Device Approval; Electrosurgery; Equipment Safety; Humans; Surgery, Plastic; United States