Cleared Special

K073140 - VITALOGIK MODEL 4000/4500

K073140 is an FDA 510(k) clearance for VITALOGIK MODEL 4000/4500, manufactured by Mennen Medical , Ltd.. The device is a Class 2 Cardiovascular device with product code DSI cleared through the Special 510(k) pathway after a 14-day FDA review.

K073140 · Mennen Medical , Ltd. · Cardiovascular device
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Nov 2007
Decision
14d
Days
Class 2
Risk

K073140 is an FDA 510(k) clearance for the VITALOGIK MODEL 4000/4500. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Mennen Medical , Ltd. (Rohovot, IL). The FDA issued a Cleared decision on November 21, 2007 after a review of 14 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 - K073140

510(k) Number K073140 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 2007
Decision Date November 21, 2007
Days to Decision 14 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
111d faster than avg
Panel avg: 125d · This submission: 14d
Pathway characteristics
Modification to existing cleared device.

DSI Device Classification - Class 2, Special Controls

Product Code DSI Detector And Alarm, Arrhythmia
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 - DSI Detector And Alarm, Arrhythmia

All 257
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