Cleared Abbreviated

ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A (K051021) - FDA 510(k) Clearance

Class II Cardiovascular device cleared through the Abbreviated 510(k) pathway - typically does not require clinical trials.

K051021 · Shanghai Lord International Trade Co., Ltd. · Cardiovascular device
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Optimized for regulatory review, auditing and printing
Jun 2005
Decision
59d
Days
Class 2
Risk

K051021 is an FDA 510(k) clearance for the ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A. Classified as Blood Pressure Cuff (product code DXQ), Class II - Special Controls.

Submitted by Shanghai Lord International Trade Co., Ltd. (Great Neck, US). The FDA issued a Cleared decision on June 20, 2005 after a review of 59 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1120 - the FDA cardiovascular device oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Shanghai Lord International Trade Co., Ltd. devices

Submission Details

510(k) Number K051021 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 22, 2005
Decision Date June 20, 2005
Days to Decision 59 days
Submission Type Abbreviated
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 125d · This submission: 59d
Pathway characteristics
Standards-based clearance path.

Device Classification

Product Code DXQ Blood Pressure Cuff
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1120
Definition A Blood Pressure Cuff Is A Device That Has An Inflatable Bladder In An Elastic Sleeve (cuff) With A Mechanism For Inflating The Bladder. The Cuff Is Used To Determine A Subject's Blood Pressure.
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 - DXQ Blood Pressure Cuff

All 197
Devices cleared under the same product code (DXQ) and FDA review panel - the closest regulatory comparables to K051021.
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