Cleared Traditional

K092650 - HEARTWAY POWER MOBILITY SCOOTER, S12 (FDA 510(k) Clearance)

Oct 2009
Decision
43d
Days
Class 2
Risk

K092650 is an FDA 510(k) clearance for the HEARTWAY POWER MOBILITY SCOOTER, S12. This device is classified as a Vehicle, Motorized 3-wheeled (Class II - Special Controls, product code INI).

Submitted by Heartway Medical Products Co., Ltd. (Hsin Chu City,,, Tw Hsq, TW). The FDA issued a Cleared decision on October 9, 2009, 43 days after receiving the submission on August 27, 2009.

This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3800.

Submission Details

510(k) Number K092650 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 2009
Decision Date October 09, 2009
Days to Decision 43 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

Device Classification

Product Code INI — Vehicle, Motorized 3-wheeled
Device Class Class II - Special Controls
CFR Regulation 21 CFR 890.3800

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