Cleared Special

K000563 - MODIFICATION TO ENVOY PATIENT MONITOR

K000563 is an FDA 510(k) clearance for MODIFICATION TO ENVOY PATIENT MONITOR, manufactured by Mennen Medical , Ltd.. The device is a Class 2 Cardiovascular device with product code MHX cleared through the Special 510(k) pathway after a 85-day FDA review.

K000563 · Mennen Medical , Ltd. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2000
Decision
85d
Days
Class 2
Risk

K000563 is an FDA 510(k) clearance for the MODIFICATION TO ENVOY PATIENT MONITOR. Classified as Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) (product code MHX), Class II - Special Controls.

Submitted by Mennen Medical , Ltd. (Rehovot, IL). The FDA issued a Cleared decision on May 17, 2000 after a review of 85 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 Mennen Medical , Ltd. devices

FDA 510(k) Submission Details - K000563

510(k) Number K000563 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 2000
Decision Date May 17, 2000
Days to Decision 85 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
40d faster than avg
Panel avg: 125d · This submission: 85d
Pathway characteristics
Modification to existing cleared device.

MHX Device Classification - Class 2, Special Controls

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 328
Devices cleared under the same product code (MHX) and FDA review panel - the closest regulatory comparables to K000563.
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