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How are breast implants studied under the Investigational Device Exemption (IDE)?
POSSIS MEDICAL FILES INVESTIGATIONAL DEVICE EXEMPTION APPLICATION MINNEAPOLIS, Sept.
In this regard, Aethlon plans to submit a formal Investigational Device Exemption (IDE) to the Food and Drug Administration (FDA) in the first quarter of 2007.
today announced that it has received an Investigational Device Exemption (IDE) from the U.
BIOPLASTY SUBMITS INVESTIGATIONAL DEVICE EXEMPTION (IDE) FOR ITS MISTI GOLD BREAST IMPLANTS ST.
Patients were enrolled in the study to assess safety and develop effective vision measures under an Investigational Device Exemption application approved by the U.
WASHINGTON -- Corindus, developer and marketer of proprietary remote control catheterization systems, announced today that it filed its Investigational Device Exemption (IDE) application for the CORRECT (Coronary Remote Control Catheterization Trial) clinical trial at the Cardiovascular Research Foundation's eighteenth annual Transcatheter Cardiovascular Therapeutics (TCT) scientific symposium in Washington, D.
a private medical device company that has developed an implantable medical device to treat high blood pressure, has received a conditional investigational device exemption (IDE) approval from the U.