Cleared Traditional

K092514 - UPPERARM DIGITAL BLOOD PRESSURE MONITOR

K092514 is the FDA 510(k) clearance for UPPERARM DIGITAL BLOOD PRESSURE MONITOR by Hangzhou Hua'An Medical & Health Instruments Co.,. It is a Class 2 Cardiovascular device (product code DXN) cleared through the Traditional 510(k) pathway after a 109-day FDA review.

K092514 · Hangzhou Hua'An Medical & Health Instruments Co., · Cardiovascular device
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Dec 2009
Decision
109d
Days
Class 2
Risk

K092514 is an FDA 510(k) clearance for the UPPERARM DIGITAL BLOOD PRESSURE MONITOR, MODEL: MB-300 SERIES. Classified as System, Measurement, Blood-pressure, Non-invasive (product code DXN), Class II - Special Controls.

Submitted by Hangzhou Hua'An Medical & Health Instruments Co., (Wuchang, Hangzhou, Zhejiang, CN). The FDA issued a Cleared decision on December 4, 2009 after a review of 109 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1130 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Hangzhou Hua'An Medical & Health Instruments Co., devices

Submission Details

510(k) Number K092514 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 2009
Decision Date December 04, 2009
Days to Decision 109 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
16d faster than avg
Panel avg: 125d · This submission: 109d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DXN System, Measurement, Blood-pressure, Non-invasive
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1130
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 - DXN System, Measurement, Blood-pressure, Non-invasive

All 504
Devices cleared under the same product code (DXN) and FDA review panel - the closest regulatory comparables to K092514.
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