Cleared Traditional

K092245 - ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100

K092245 is an FDA 510(k) clearance for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, manufactured by Honsun (Nantong) Co., Ltd.. The device is a Class 2 Cardiovascular device with product code DXQ cleared through the Traditional 510(k) pathway after a 92-day FDA review.

K092245 · Honsun (Nantong) Co., Ltd. · Cardiovascular device
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Optimized for regulatory review, auditing and printing
Oct 2009
Decision
92d
Days
Class 2
Risk

K092245 is an FDA 510(k) clearance for the ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100. Classified as Blood Pressure Cuff (product code DXQ), Class II - Special Controls.

Submitted by Honsun (Nantong) Co., Ltd. (Jiangsu, CN). The FDA issued a Cleared decision on October 28, 2009 after a review of 92 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1120 - 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 Honsun (Nantong) Co., Ltd. devices

FDA 510(k) Submission Details - K092245

510(k) Number K092245 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 2009
Decision Date October 28, 2009
Days to Decision 92 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
33d faster than avg
Panel avg: 125d · This submission: 92d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXQ Device Classification - Class 2, Special Controls

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 158
Devices cleared under the same product code (DXQ) and FDA review panel - the closest regulatory comparables to K092245.
HEINE GAMMA G7
K101892 · Heine Optotechnik GmbH & Co. KG · Aug 2010
SOLARIS REUSABLE AND DISPOSABLE BLOOD PRESSURE CUFFS
K101972 · Solaris Medical Technology, Inc. · Jul 2010
NBP CUFF
K092999 · Draeger Medical AG & Co. KG · Nov 2009
LARGE FACE ANEROID SPHYGMOMANOMETER, WALL MODEL, DESK MODEL, MOBILE STAND MODEL, MODEL 41XX, 42XX, 43XX
K092604 · Trimline Medical Products Corp. · Oct 2009
CAREMATE SPHYGMOMANOMETER WITH STETHOSCOPE
K090014 · Caremate Medical Device Co., Ltd. · Apr 2009
DEVON ACCUBP CUFF
K090664 · Devon Medical, Inc. · Mar 2009