Cleared Traditional

K080983 - PROVENT NASAL CANNULA

K080983 is an FDA 510(k) clearance for PROVENT NASAL CANNULA, manufactured by Ventus Medical, Inc.. The device is a Class 2 Anesthesiology device with product code MNR cleared through the Traditional 510(k) pathway after a 122-day FDA review.

K080983 · Ventus Medical, Inc. · Anesthesiology device
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Aug 2008
Decision
122d
Days
Class 2
Risk

K080983 is an FDA 510(k) clearance for the PROVENT NASAL CANNULA. Classified as Ventilatory Effort Recorder (product code MNR), Class II - Special Controls.

Submitted by Ventus Medical, Inc. (Belmont, US). The FDA issued a Cleared decision on August 7, 2008 after a review of 122 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.2375 - the FDA anesthesiology and respiratory device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Ventus Medical, Inc. devices

FDA 510(k) Submission Details - K080983

510(k) Number K080983 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 2008
Decision Date August 07, 2008
Days to Decision 122 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
18d faster than avg
Panel avg: 140d · This submission: 122d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNR Device Classification - Class 2, Special Controls

Product Code MNR Ventilatory Effort Recorder
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.2375
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Anesthesiology devices follow this clearance model.

Regulatory Peers - MNR Ventilatory Effort Recorder

All 65
Devices cleared under the same product code (MNR) and FDA review panel - the closest regulatory comparables to K080983.
SOMNOLYZER 24X7
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GALAXY
K083874 · Respironics Inc., Sleep & Home Respiratory Group · Jan 2009
CADWELL EASYNET NASAL PRESSURE MODULE
K061705 · Cadwell Laboratories, Inc. · Nov 2006
STARDUST II
K052573 · Respironics, Inc. · Dec 2005
BI-NAPS NASAL AIRFLOW AND SNORE TRANSDUCER
K051313 · Salter Labs · Sep 2005