Cleared Traditional

K071773 - CPAP NASAL MASK WITH PILLOWS

K071773 is an FDA 510(k) clearance for CPAP NASAL MASK WITH PILLOWS, manufactured by Lifesource. The device is a Class 2 Anesthesiology device with product code BZD cleared through the Traditional 510(k) pathway after a 75-day FDA review.

K071773 · Lifesource · Anesthesiology device
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Sep 2007
Decision
75d
Days
Class 2
Risk

K071773 is an FDA 510(k) clearance for the CPAP NASAL MASK WITH PILLOWS. Classified as Ventilator, Non-continuous (respirator) (product code BZD), Class II - Special Controls.

Submitted by Lifesource (Bonita Springs, US). The FDA issued a Cleared decision on September 12, 2007 after a review of 75 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 Lifesource devices

FDA 510(k) Submission Details - K071773

510(k) Number K071773 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 29, 2007
Decision Date September 12, 2007
Days to Decision 75 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
65d faster than avg
Panel avg: 140d · This submission: 75d
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 K071773.
PERFORMAX TOTAL FACE MASK
K072592 · Respironics Inc., Sleep & Home Respiratory Group · Dec 2007
MIRAGE MICRO
K072940 · Resmed, Ltd. · Dec 2007
MIRAGE MICRO
K071808 · Resmed, Ltd. · Oct 2007
RESTRAXX DATA CENTRE, MODEL R10
K070746 · Resmed, Ltd. · Jul 2007
VPAP AUTO WITH H3I
K071171 · Resmed, Ltd. · Jul 2007
APEX MEDICAL XT1 CPAP, MODEL 9S-005
K070609 · Apex Medical Corp. · May 2007