Cleared Special

K040357 - M3290A INTELLIVUE INFORMATION CENTER SO...

K040357 is the FDA 510(k) clearance for M3290A INTELLIVUE INFORMATION CENTER SO... by Philips Medical Systems, Inc.. It is a Class 2 Cardiovascular device (product code MHX) cleared through the Special 510(k) pathway after a 19-day FDA review.

K040357 · Philips Medical Systems, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2004
Decision
19d
Days
Class 2
Risk

K040357 is an FDA 510(k) clearance for the M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE F.O AND THE M4840A TELE.... Classified as Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) (product code MHX), Class II - Special Controls.

Submitted by Philips Medical Systems, Inc. (Andover, US). The FDA issued a Cleared decision on March 3, 2004 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1025 - 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 Philips Medical Systems, Inc. devices

Submission Details

510(k) Number K040357 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 13, 2004
Decision Date March 03, 2004
Days to Decision 19 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
106d faster than avg
Panel avg: 125d · This submission: 19d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1025
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 - MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)

All 300
Devices cleared under the same product code (MHX) and FDA review panel - the closest regulatory comparables to K040357.
M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE E.01 AND INTELLIVUE CLINICAL NETWORK ON VLAN
K040955 · Philips Medical Systems, Inc. · May 2004
INFINITY GAMMA
K041087 · Draeger Medical Systems, Inc. · May 2004
INFINITY MODULAR MONITORS VF4 MODIFICATIONS
K033694 · Draeger Medical Systems, Inc. · Mar 2004
PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50
K040304 · Philips Medizin Systeme Boeblingen GmbH · Mar 2004
ENVOY PATIENT MONITOR
K030722 · Mennen Medical, Inc. · Feb 2004
SOLAR 9500 INFORMATION MONITOR
K033964 · Ge Medical Systems Information Technologies · Jan 2004