Agilent Technologies | 合法醫療器材資訊網
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2001年5月3日—AgilentTechnologiesInc.(NYSE:A),theleadingworldwidemanufacturerofautomaticexternaldefibrillators(AEDs),todayannouncedthatit ...
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PALO ALTO, Calif.--(BW HealthWire)--May 3, 2001--
Innovative Pediatric Pads Enable Use of an AED to
Save the Lives of the Youngest Victims of Sudden Cardiac Arrest
Agilent Technologies Inc. (NYSE: A), the leading worldwide manufacturer of automatic external defibrillators (AEDs), today announced that it has become the first company to receive 510(k) clearance from the Food and Drug Administration (FDA) to market its Heartstream FR2 AED for use on children. The Heartstream FR2 AED, when equipped with specially designed defibrillation pads, can be used on infants and children under age 8.
Sudden cardiac arrest (SCA) is a leading cause of death in the United States, striking approximately 225,000 Americans annually, including small children. AEDs provide definitive treatment by delivering an electric shock to the heart that can re-establish a regular heartbeat. Howeve...
Agilent Heartstream FR2 | 合法醫療器材資訊網
Agilent Heartstream FR2 AED Defibrillator | 合法醫療器材資訊網
Agilent M3860A | 合法醫療器材資訊網
Agilent M47 5A Heartstream ;L DefibrillatorMonitor | 合法醫療器材資訊網
Agilent Technologies | 合法醫療器材資訊網
Agilent Technologies | 合法醫療器材資訊網
COMPATIBLE PADS for defibrillator Agilent | 合法醫療器材資訊網
HeartStart FR2 Series Defibrillators | 合法醫療器材資訊網
Phillips Agilent M3860A Heartstream HeartStart Fr2 AED ... | 合法醫療器材資訊網
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【心臟電擊蘇復器】許可證字號:衛署醫器輸字第004030號
器材品名:心臟電擊蘇復器許可證字號:衛署醫器輸字第004030號註銷狀態:已註銷註銷日期:2007/07/20註銷理由:許可證已逾有效期...