Cleared Abbreviated

K142554 - Revolution Full Face Mask

K142554 is an FDA 510(k) clearance for Revolution Full Face Mask, manufactured by Respironics, Inc.. The device is a Class 2 Anesthesiology device with product code BZD cleared through the Abbreviated 510(k) pathway after a 120-day FDA review.

K142554 · Respironics, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2015
Decision
120d
Days
Class 2
Risk

K142554 is an FDA 510(k) clearance for the Revolution Full Face Mask. Classified as Ventilator, Non-continuous (respirator) (product code BZD), Class II - Special Controls.

Submitted by Respironics, Inc. (Murrysville, US). The FDA issued a Cleared decision on January 9, 2015 after a review of 120 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5905 - the FDA anesthesiology and respiratory device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Respironics, Inc. devices

FDA 510(k) Submission Details - K142554

510(k) Number K142554 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 2014
Decision Date January 09, 2015
Days to Decision 120 days
Submission Type Abbreviated
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 140d · This submission: 120d
Pathway characteristics
Standards-based clearance path.

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 285
Devices cleared under the same product code (BZD) and FDA review panel - the closest regulatory comparables to K142554.
CPAP Cannulaide
K143700 · Salter Labs · Aug 2015
Darlinghurst Vented, Darlinghurst NV-AAV
K143603 · Resmed, Ltd. · May 2015
TI NASAL MASK
K140980 · Respironics, Inc. · Feb 2015
SIMPLE T YOUTH NASAL MASK
K140268 · Respironics, Inc. · Oct 2014
APEX MEDICAL CORP. ICH CPAP WITH PVA 9S-007XXX SERIES
K141522 · Apex Medical Corp. · Oct 2014
S9 GREENHILLS
K140279 · Resmed, Ltd. · Jul 2014