Cleared Special

K041942 - M2376A DEVICELINK SYSTEM

K041942 is an FDA 510(k) clearance for M2376A DEVICELINK SYSTEM, manufactured by Phillips Medical Systems. The device is a Class 2 Cardiovascular device with product code MWI cleared through the Special 510(k) pathway after a 4-day FDA review.

K041942 · Phillips Medical Systems · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2004
Decision
4d
Days
Class 2
Risk

K041942 is an FDA 510(k) clearance for the M2376A DEVICELINK SYSTEM. Classified as Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) (product code MWI), Class II - Special Controls.

Submitted by Phillips Medical Systems (Boblingen, DE). The FDA issued a Cleared decision on July 23, 2004 after a review of 4 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2300 - the FDA cardiovascular device oversight 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. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Phillips Medical Systems devices

FDA 510(k) Submission Details - K041942

510(k) Number K041942 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 2004
Decision Date July 23, 2004
Days to Decision 4 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
121d faster than avg
Panel avg: 125d · This submission: 4d
Pathway characteristics
Modification to existing cleared device.

MWI Device Classification - Class 2, Special Controls

Product Code MWI Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2300
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - MWI Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms)

All 175
Devices cleared under the same product code (MWI) and FDA review panel - the closest regulatory comparables to K041942.
STELLAR 404 MONITORING SYSTEM
K042560 · Larsen & Toubro Limited · Oct 2004
8600 VITAL SIGNS MONITOR
K042569 · Criticare Systems, Inc. · Sep 2004
TRIO MONITOR
K041907 · Datascope Corp. · Jul 2004
C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054
K041376 · Analogic Corp. · Jul 2004
MODIFICATION TO UNITY NETWORK ID
K040559 · Ge Medical Systems Information Technologies · Jun 2004
MODIFICATION TO M2376A DEVICELINK SYSTEM
K041401 · Philips Medical Systems · Jun 2004