Cleared Traditional

K092154 - HEARTWAY POWER MOBILITY SCOOTER

K092154 is an FDA 510(k) clearance for HEARTWAY POWER MOBILITY SCOOTER, manufactured by Heartway Medical Products Co., Ltd.. The device is a Class 2 Physical Medicine device with product code INI cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K092154 · Heartway Medical Products Co., Ltd. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2009
Decision
67d
Days
Class 2
Risk

K092154 is an FDA 510(k) clearance for the HEARTWAY POWER MOBILITY SCOOTER, S9. Classified as Vehicle, Motorized 3-wheeled (product code INI), Class II - Special Controls.

Submitted by Heartway Medical Products Co., Ltd. (Hsin-Chu City, TW). The FDA issued a Cleared decision on September 21, 2009 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3800 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Heartway Medical Products Co., Ltd. devices

FDA 510(k) Submission Details - K092154

510(k) Number K092154 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 16, 2009
Decision Date September 21, 2009
Days to Decision 67 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
48d faster than avg
Panel avg: 115d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

INI Device Classification - Class 2, Special Controls

Product Code INI Vehicle, Motorized 3-wheeled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3800
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - INI Vehicle, Motorized 3-wheeled

All 116
Devices cleared under the same product code (INI) and FDA review panel - the closest regulatory comparables to K092154.
HEARTWAY LIGHTWEIGHT POWER MOBILITY SCOOTER, S34
K101142 · Heartway Medical Products Co., Ltd. · May 2010
HEARTWAY POWER MOBILITY SCOOTER, S11
K101143 · Heartway Medical Products Co., Ltd. · May 2010
HEARTWAY POWER MOBILITY SCOOTER, S12
K092650 · Heartway Medical Products Co., Ltd. · Oct 2009
HEARTWAY POWER MOBILITY SCOOTER, S8
K092155 · Heartway Medical Products Co., Ltd. · Sep 2009
WU'S 3 WHEELED ELECTRICAL SCOOTER, WT-T3H
K091212 · Wu'S Tech Co., Ltd. · May 2009
WU'S 4-WHEELED NEO SCOOTER, WT-M3A
K082963 · Wu'S Tech Co., Ltd. · Nov 2008