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FDA 510(k)

EPW FOLDABLE POWER WHEELCHAIR, EPW-03

K-Number: K033206 · 2003-12-18

Decision Date2003-12-18
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EPW FOLDABLE POWER WHEELCHAIR, EPW-03 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 2003-12-18 under 510(k) number K033206. 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 EPW FOLDABLE POWER WHEELCHAIR, EPW-03?

EPW FOLDABLE POWER WHEELCHAIR, EPW-03 is a medical device that received FDA 510(k) clearance on 2003-12-18. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K033206.

When did EPW FOLDABLE POWER WHEELCHAIR, EPW-03 receive FDA 510(k) clearance?

EPW FOLDABLE POWER WHEELCHAIR, EPW-03 received FDA 510(k) clearance on 2003-12-18, under 510(k) number K033206.

Who is the listed applicant for EPW FOLDABLE POWER WHEELCHAIR, EPW-03?

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 EPW FOLDABLE POWER WHEELCHAIR, EPW-03?

The FDA product code for EPW FOLDABLE POWER WHEELCHAIR, EPW-03 is ITI.

Related Clinical Trials

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.

Other records listing Emg Technology Co., Ltd. as applicant

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.

View all 11 devices →

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.

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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