Cleared Traditional

K131572 - MICRO AMBULATORY ECG RECORDER

K131572 is an FDA 510(k) clearance for MICRO AMBULATORY ECG RECORDER, manufactured by Dimetek Digital Medical Technologies, Ltd.. The device is a Class 2 Cardiovascular device with product code DPS cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K131572 · Dimetek Digital Medical Technologies, Ltd. · Cardiovascular device
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Jul 2013
Decision
52d
Days
Class 2
Risk

K131572 is an FDA 510(k) clearance for the MICRO AMBULATORY ECG RECORDER. Classified as Electrocardiograph (product code DPS), Class II - Special Controls.

Submitted by Dimetek Digital Medical Technologies, Ltd. (Shekou, Shenzhen, CN). The FDA issued a Cleared decision on July 22, 2013 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2340 - 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 Dimetek Digital Medical Technologies, Ltd. devices

FDA 510(k) Submission Details - K131572

510(k) Number K131572 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 31, 2013
Decision Date July 22, 2013
Days to Decision 52 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 125d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

DPS Device Classification - Class 2, Special Controls

Product Code DPS Electrocardiograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2340
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 - DPS Electrocardiograph

All 309
Devices cleared under the same product code (DPS) and FDA review panel - the closest regulatory comparables to K131572.
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