Cleared Traditional

K113815 - RESSCAN

K113815 is the FDA 510(k) clearance for RESSCAN by Resmed, Ltd.. It is a Class 2 Anesthesiology device (product code MNS) cleared through the Traditional 510(k) pathway after a 95-day FDA review.

K113815 · Resmed, Ltd. · Anesthesiology device
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Mar 2012
Decision
95d
Days
Class 2
Risk

K113815 is an FDA 510(k) clearance for the RESSCAN. Classified as Ventilator, Continuous, Non-life-supporting (product code MNS), Class II - Special Controls.

Submitted by Resmed, Ltd. (San Diego, US). The FDA issued a Cleared decision on March 27, 2012 after a review of 95 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 Resmed, Ltd. devices

Submission Details

510(k) Number K113815 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 23, 2011
Decision Date March 27, 2012
Days to Decision 95 days
Submission Type Traditional
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
45d faster than avg
Panel avg: 140d · This submission: 95d
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 35
Devices cleared under the same product code (MNS) and FDA review panel - the closest regulatory comparables to K113815.
VPAP S-A
K122324 · Resmed, Ltd. · Nov 2012
VPAP TX
K113714 · Resmed, Ltd. · May 2012
VPAP ST-A
K113288 · Resmed, Ltd. · Mar 2012
BIPAP A 30 VENTILATORY SUPPORT SYSTEM
K113053 · Respironics, Inc. · Feb 2012
VPAP TX
K112914 · Resmed, Ltd. · Dec 2011
BIPAP AVAPS VENTILATORY SUPPORT SYSTEM
K102465 · Respironics, Inc. · Mar 2011