FDA 510(k) Applications Submitted by VENTUS MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K120665 03/05/2012 INVENT SNORING DEVICE VENTUS MEDICAL, INC.
K080983 04/07/2008 PROVENT NASAL CANNULA VENTUS MEDICAL, INC.
K071560 06/07/2007 PROVENT NASAL DILATOR, MODEL BR2 VENTUS MEDICAL, INC.
K090398 02/17/2009 PROVENT PROFESSIONAL SLEEP APNEA THERAPY VENTUS MEDICAL, INC.
K102404 08/24/2010 PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50) VENTUS MEDICAL, INC.


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