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FDA 510(k)

MIDDLE WHEEL DRIVE POWER CHAIR, CWD01

K-Number: K062888 · 2006-10-24

ApplicantEmg Technology Co., Ltd.
Decision Date2006-10-24
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MIDDLE WHEEL DRIVE POWER CHAIR, CWD01 is the device name listed in this FDA 510(k) record. The listed applicant is Emg Technology Co., Ltd.. It received FDA 510(k) clearance on 2006-10-24 under 510(k) number K062888. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDDLE WHEEL DRIVE POWER CHAIR, CWD01?

MIDDLE WHEEL DRIVE POWER CHAIR, CWD01 is a medical device that received FDA 510(k) clearance on 2006-10-24. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K062888.

When did MIDDLE WHEEL DRIVE POWER CHAIR, CWD01 receive FDA 510(k) clearance?

MIDDLE WHEEL DRIVE POWER CHAIR, CWD01 received FDA 510(k) clearance on 2006-10-24, under 510(k) number K062888.

Who is the listed applicant for MIDDLE WHEEL DRIVE POWER CHAIR, CWD01?

The FDA 510(k) record lists Emg Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDDLE WHEEL DRIVE POWER CHAIR, CWD01?

The FDA product code for MIDDLE WHEEL DRIVE POWER CHAIR, CWD01 is ITI.

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Related Devices (Code: ITI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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