Cleared Special

K122712 - DIGITAL ELECTROCARDIOGRAPH

K122712 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 51-day FDA review.

K122712 · Shenzhen Biocare Electronics Co., Ltd. · Cardiovascular device
Download Printable Device Report (PDF)
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Oct 2012
Decision
51d
Days
Class 2
Risk

K122712 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 October 25, 2012 after a review of 51 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 - K122712

510(k) Number K122712 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 2012
Decision Date October 25, 2012
Days to Decision 51 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
74d faster than avg
Panel avg: 125d · This submission: 51d
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
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