Nuocande Plastic Manual Wheelchair Model NKD L07

FDA 510(k) K151797 · Ningbo Lecount Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK151797

Submission

Device name
Nuocande Plastic Manual Wheelchair Model NKD L07
Applicant
Ningbo Lecount Medical Technology Co., Ltd.
Ningbo, CN
Received
July 2, 2015
Decision date
August 25, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IOR – Wheelchair, Mechanical
Device class
Class I (low risk)
Regulation
21 CFR 890.3850
Specialty
Physical Medicine

A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position” to mean the device type is intended to provide mobility to individuals who have mobility impairments and/or require an assistive device for mobility.

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K254141Manual Wheelchair (DY01903(2))IOR · Traditional Guangdong Dayang Medical Technology Co., Ltd.05/21/2026SE
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Questions and answers

When was Nuocande Plastic Manual Wheelchair Model NKD L07 cleared by the FDA?

Nuocande Plastic Manual Wheelchair Model NKD L07 (K151797) received a 510(k) decision of Substantially Equivalent on August 25, 2015, 54 days after the submission was received.

What is the product code of K151797?

The FDA product code is IOR – Wheelchair, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3850.