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FDA 510(k)

SINON POWER WHEELCHAIR, SN-P401

K-Number: K040320 · 2004-03-12

ApplicantSinon Corporation
Decision Date2004-03-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SINON POWER WHEELCHAIR, SN-P401 is the device name listed in this FDA 510(k) record. The listed applicant is Sinon Corporation. It received FDA 510(k) clearance on 2004-03-12 under 510(k) number K040320. 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 SINON POWER WHEELCHAIR, SN-P401?

SINON POWER WHEELCHAIR, SN-P401 is a medical device that received FDA 510(k) clearance on 2004-03-12. The listed applicant is Sinon Corporation. The 510(k) number is K040320.

When did SINON POWER WHEELCHAIR, SN-P401 receive FDA 510(k) clearance?

SINON POWER WHEELCHAIR, SN-P401 received FDA 510(k) clearance on 2004-03-12, under 510(k) number K040320.

Who is the listed applicant for SINON POWER WHEELCHAIR, SN-P401?

The FDA 510(k) record lists Sinon Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SINON POWER WHEELCHAIR, SN-P401?

The FDA product code for SINON POWER WHEELCHAIR, SN-P401 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.

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Other records listing Sinon Corporation 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.

K041465SINON SN-L402 LIGHTWEIGHT WHEELCHAIRK040319SINON POWER WHEELCHAIR, SN-W401

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

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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