Cleared Traditional

K071689 - DEVILBISS INTELLIPAP MODEL DV 5 SERIES

K071689 is an FDA 510(k) clearance for DEVILBISS INTELLIPAP MODEL DV 5 SERIES, manufactured by Sunrise Medical. The device is a Class 2 Anesthesiology device with product code BZD cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K071689 · Sunrise Medical · Anesthesiology device
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Sep 2007
Decision
79d
Days
Class 2
Risk

K071689 is an FDA 510(k) clearance for the DEVILBISS INTELLIPAP MODEL DV 5 SERIES. Classified as Ventilator, Non-continuous (respirator) (product code BZD), Class II - Special Controls.

Submitted by Sunrise Medical (Somerset, US). The FDA issued a Cleared decision on September 7, 2007 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5905 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Sunrise Medical devices

FDA 510(k) Submission Details - K071689

510(k) Number K071689 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 20, 2007
Decision Date September 07, 2007
Days to Decision 79 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 140d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BZD Device Classification - Class 2, Special Controls

Product Code BZD Ventilator, Non-continuous (respirator)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5905
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 - BZD Ventilator, Non-continuous (respirator)

All 307
Devices cleared under the same product code (BZD) and FDA review panel - the closest regulatory comparables to K071689.
PERFORMAX TOTAL FACE MASK
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K070609 · Apex Medical Corp. · May 2007