Cleared Special

K102502 - GOLIFE NASAL MASK

K102502 is an FDA 510(k) clearance for GOLIFE NASAL MASK, manufactured by Respironics, Inc.. The device is a Class 2 Anesthesiology device with product code BZD cleared through the Special 510(k) pathway after a 112-day FDA review.

K102502 · Respironics, Inc. · Anesthesiology device
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Dec 2010
Decision
112d
Days
Class 2
Risk

K102502 is an FDA 510(k) clearance for the GOLIFE NASAL MASK. Classified as Ventilator, Non-continuous (respirator) (product code BZD), Class II - Special Controls.

Submitted by Respironics, Inc. (Pittsburgh, US). The FDA issued a Cleared decision on December 22, 2010 after a review of 112 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Respironics, Inc. devices

FDA 510(k) Submission Details - K102502

510(k) Number K102502 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 01, 2010
Decision Date December 22, 2010
Days to Decision 112 days
Submission Type Special
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
28d faster than avg
Panel avg: 140d · This submission: 112d
Pathway characteristics
Modification to existing cleared device.

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 K102502.
GOLIFE NASAL MASK
K110008 · Respironics, Inc. · Feb 2011
S9 VPAP ST WITH H5I
K102513 · Resmed, Ltd. · Jan 2011
MIRAGE FX
K102746 · Resmed, Ltd. · Dec 2010
PIXI PEDIATRIC MASK
K102224 · Resmed, Ltd. · Dec 2010
FISHER & PAYKEL HEALTHCARE BUBBLE CPAP SYSTEM
K100011 · Fisher &Paykel Healthcare , Ltd. · Oct 2010
MIRAGE MICRO MODEL 16333 (S), 16334 (M&L), 16335 (LW & XL)
K100772 · Resmed, Ltd. · Jun 2010