Cleared Special

K112431 - DIGITAL ELECTROCARDIOGRAPH

K112431 is an FDA 510(k) clearance for DIGITAL ELECTROCARDIOGRAPH, manufactured by Shenzhen Biocare Electronics Co., Ltd.. The device is a Class 2 Cardiovascular device with product code DPS cleared through the Special 510(k) pathway after a 30-day FDA review.

K112431 · Shenzhen Biocare Electronics Co., Ltd. · Cardiovascular device
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Sep 2011
Decision
30d
Days
Class 2
Risk

K112431 is an FDA 510(k) clearance for the DIGITAL ELECTROCARDIOGRAPH. Classified as Electrocardiograph (product code DPS), Class II - Special Controls.

Submitted by Shenzhen Biocare Electronics Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on September 22, 2011 after a review of 30 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. 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 Shenzhen Biocare Electronics Co., Ltd. devices

FDA 510(k) Submission Details - K112431

510(k) Number K112431 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 23, 2011
Decision Date September 22, 2011
Days to Decision 30 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 125d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

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 270
Devices cleared under the same product code (DPS) and FDA review panel - the closest regulatory comparables to K112431.
RSCRIBE ELECTROCARDIOGRAPH
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