Cleared Traditional

K000882 - DATEX-OHMEDA CS/3 TELEMETRY SYSTEM

K000882 is an FDA 510(k) clearance for DATEX-OHMEDA CS/3 TELEMETRY SYSTEM, manufactured by Datex-Ohmeda. The device is a Class 2 Cardiovascular device with product code MHX cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K000882 · Datex-Ohmeda · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2000
Decision
77d
Days
Class 2
Risk

K000882 is an FDA 510(k) clearance for the DATEX-OHMEDA CS/3 TELEMETRY SYSTEM. Classified as Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) (product code MHX), Class II - Special Controls.

Submitted by Datex-Ohmeda (Tewksbury, US). The FDA issued a Cleared decision on June 5, 2000 after a review of 77 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Datex-Ohmeda devices

FDA 510(k) Submission Details - K000882

510(k) Number K000882 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 20, 2000
Decision Date June 05, 2000
Days to Decision 77 days
Submission Type Traditional
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
48d faster than avg
Panel avg: 125d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 319
Devices cleared under the same product code (MHX) and FDA review panel - the closest regulatory comparables to K000882.
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AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)
K000815 · Datex-Ohmeda · Jun 2000
ST/AR ST AND ARRHYTHMIA SOFTWARE
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CS/3 CRITICAL CARE MONITOR WITH S-ICU99(A)
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DATEX-OHMEDA NE12STPR MODULE (MODEL FAMILY M-NE12STPR)
K993608 · Datex-Ohmeda, Inc. · Apr 2000