Cleared Traditional

K071702 - BREAS VIVO BILEVEL SYSTEM

K071702 is an FDA 510(k) clearance for BREAS VIVO BILEVEL SYSTEM, manufactured by Breas Medical AB. The device is a Class 2 Anesthesiology device with product code MNT cleared through the Traditional 510(k) pathway after a 239-day FDA review.

K071702 · Breas Medical AB · Anesthesiology device
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Feb 2008
Decision
239d
Days
Class 2
Risk

K071702 is an FDA 510(k) clearance for the BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 40. Classified as Ventilator, Continuous, Minimal Ventilatory Support, Facility Use (product code MNT), Class II - Special Controls.

Submitted by Breas Medical AB (Molnlycke, SE). The FDA issued a Cleared decision on February 15, 2008 after a review of 239 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5895 - 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 Breas Medical AB devices

FDA 510(k) Submission Details - K071702

510(k) Number K071702 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 21, 2007
Decision Date February 15, 2008
Days to Decision 239 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
99d slower than avg
Panel avg: 140d · This submission: 239d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNT Device Classification - Class 2, Special Controls

Product Code MNT Ventilator, Continuous, Minimal Ventilatory Support, Facility Use
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5895
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 - MNT Ventilator, Continuous, Minimal Ventilatory Support, Facility Use

All 16
Devices cleared under the same product code (MNT) and FDA review panel - the closest regulatory comparables to K071702.
F&P Nivairo RT047 Vented Hospital Full Face Mask, Anti-Asphyxiation Valve Version
K191624 · Fisher & Paykel Healthcare Limited · Mar 2020
BIPAP A 40 VENTILATORY SUPPORT SYSTEM
K121623 · Respironics, Inc. · Dec 2012
V60 VENTILATOR WITH PPV AND AUTO-TRAK+ SOFTWARE OPTIONS
K102985 · Respironics, Inc. · Apr 2011
ACUTE CARE FACE MASK, MODEL RT040
K060044 · Fisher &Paykel Healthcare , Ltd. · Apr 2006
STICK-ON DISPOSABLE NASAL MASK, MODEL 312174, 1001964
K990574 · Respironics, Inc. · May 1999
BIPAP VISION VENTILATORY SUPPORT
K982454 · Respironics, Inc. · Nov 1998