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Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems (US Food and Drug Administration Regulation) (FDA) (
The Law Library
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Createspace Independent Publishing Platform
· Paperback
Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems (US Food and Drug Administration Regulation) (FDA) ( - The Law Library
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Synopsis "Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems (US Food and Drug Administration Regulation) (FDA) ("
Effective Date of Requirement for Premarket Approval for Automated External Defibrillator Systems (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 (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 issuing a final order to require 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 (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section
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The book is written in English.
The binding of this edition is Paperback.
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