Cleared Traditional

K111378 - OXIMETRY INTERFACE KIT (FDA 510(k) Clearance)

Class II Anesthesiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K111378 · Philips Respironics, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2011
Decision
140d
Days
Class 2
Risk

K111378 is an FDA 510(k) clearance for the OXIMETRY INTERFACE KIT. Classified as Ventilator, Continuous, Non-life-supporting (product code MNS), Class II - Special Controls.

Submitted by Philips Respironics, Inc. (Murrysville, US). The FDA issued a Cleared decision on October 4, 2011 after a review of 140 days - within the typical 510(k) review window.

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 Philips Respironics, Inc. devices

Submission Details

510(k) Number K111378 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 17, 2011
Decision Date October 04, 2011
Days to Decision 140 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
1d slower than avg
Panel avg: 139d · This submission: 140d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MNS Ventilator, Continuous, Non-life-supporting
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 - MNS Ventilator, Continuous, Non-life-supporting

All 46
Devices cleared under the same product code (MNS) and FDA review panel - the closest regulatory comparables to K111378.
myAir
K251889 · ResMed Corp · Apr 2026
BreathePal Bilevel (GFM50-MD2201)
K252078 · Compal Electronics, Inc. · Mar 2026
Mariana Minerva
K251661 · Resmed Pty , Ltd. · Feb 2026
Vivo 1, Vivo 2
K240778 · Breas Medical AB · Dec 2024
ReddyPort Elbow
K231064 · Smd Manufacturing, LLC · Jul 2023
BPAP System
K213169 · BMC Medical Co., Ltd. · Dec 2022