Name: Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Reg (en Inglés)
Price: 84319.00 COP
Availability: InStock
Author: The Law Library
ISBN: 9781727301663

portada Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Reg (en Inglés)

Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Reg (en Inglés)

Formato

Libro Físico

Autor

The Law Library

Editorial

Createspace

Idioma

Inglés

N° páginas

Encuadernación

Tapa Blanda

Dimensiones

25.4 x 17.8 x 0.2 cm

Peso

0.07 kg.

ISBN13

9781727301663

Categorías

Teoría general del derecho

Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Reg (en Inglés)

The Law Library (Autor) · Createspace · Tapa Blanda

Libro Nuevo Importado

Envío: 18 a 24 días háb.

$ 168.639$ 84.319

-50%

Costos de importación incluídos en el precio ✅

Libro Nuevo

Quedan más de 100 unidades

$ 84.319

Llega entre el 19 Ago y el 28 Ago a Bogota, Cundinamarca. Seleccionar ubicación

Agregar a lista de deseos

Reseña del libro "Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Reg (en Inglés)"

Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library presents the complete text of the Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Regulation) (FDA) (2018 Edition). Updated as of May 29, 2018 The Food and Drug Administration (FDA or the Agency) is republishing in its entirety a final order entitled "Effective Date of Requirement for Premarket Approval for Automated External Defibrillator" that published in the Federal Register on January 29, 2015 (80 FR 4783). FDA is republishing to correct an inadvertent omission of a comment regarding adverse tissue reaction as a risk to health and the Agency's response to that comment. The final order requires the filing of premarket approval applications (PMA) for automated external defibrillator (AED) systems, which consist of an AED and those AED accessories necessary for the AED to detect and interpret an electrocardiogram and deliver an electrical shock (e.g., pad electrodes, batteries, adapters, and hardware keys for pediatric use). This book contains: - The complete text of the Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems - Republication (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section