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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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