Cleared Traditional

K121367 - ZOLL PROPAQ XM

K121367 is the FDA 510(k) clearance for ZOLL PROPAQ XM by ZOLL Medical Corporation. It is a Class 2 Cardiovascular device (product code MHX) cleared through the Traditional 510(k) pathway after a 45-day FDA review.

K121367 · ZOLL Medical Corporation · Cardiovascular device
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Optimized for regulatory review, auditing and printing
Jun 2012
Decision
45d
Days
Class 2
Risk

K121367 is an FDA 510(k) clearance for the ZOLL PROPAQ XM. Classified as Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) (product code MHX), Class II - Special Controls.

Submitted by ZOLL Medical Corporation (Chelsmford, US). The FDA issued a Cleared decision on June 21, 2012 after a review of 45 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 ZOLL Medical Corporation devices

Submission Details

510(k) Number K121367 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 2012
Decision Date June 21, 2012
Days to Decision 45 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
80d faster than avg
Panel avg: 125d · This submission: 45d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 275
Devices cleared under the same product code (MHX) and FDA review panel - the closest regulatory comparables to K121367.
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K120616 · Spacelabs Medical, Inc. · Mar 2012
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K113798 · Draeger Medical Systems, Inc. · Mar 2012