Cleared Special

K011824 - AGILENT M2636B TELEMON B MONITOR (TELEMON B)

K011824 is an FDA 510(k) clearance for AGILENT M2636B TELEMON B MONITOR (TELEM..., manufactured by Agilent Technologies, Inc.. The device is a Class 2 Cardiovascular device with product code DSI cleared through the Special 510(k) pathway after a 21-day FDA review.

K011824 · Agilent Technologies, Inc. · Cardiovascular device
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Jul 2001
Decision
21d
Days
Class 2
Risk

K011824 is an FDA 510(k) clearance for the AGILENT M2636B TELEMON B MONITOR (TELEMON B). Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Agilent Technologies, Inc. (Andover, US). The FDA issued a Cleared decision on July 2, 2001 after a review of 21 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 Agilent Technologies, Inc. devices

FDA 510(k) Submission Details - K011824

510(k) Number K011824 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 11, 2001
Decision Date July 02, 2001
Days to Decision 21 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
104d faster than avg
Panel avg: 125d · This submission: 21d
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 302
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