Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FORYOU POWERED WHEELCHAIR, MODEL FC-100

K-Number: K061693 · 2006-07-06

ApplicantForyou Technology Co., Ltd.
Decision Date2006-07-06
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORYOU POWERED WHEELCHAIR, MODEL FC-100 is the device name listed in this FDA 510(k) record. The listed applicant is Foryou Technology Co., Ltd.. It received FDA 510(k) clearance on 2006-07-06 under 510(k) number K061693. 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 FORYOU POWERED WHEELCHAIR, MODEL FC-100?

FORYOU POWERED WHEELCHAIR, MODEL FC-100 is a medical device that received FDA 510(k) clearance on 2006-07-06. The listed applicant is Foryou Technology Co., Ltd.. The 510(k) number is K061693.

When did FORYOU POWERED WHEELCHAIR, MODEL FC-100 receive FDA 510(k) clearance?

FORYOU POWERED WHEELCHAIR, MODEL FC-100 received FDA 510(k) clearance on 2006-07-06, under 510(k) number K061693.

Who is the listed applicant for FORYOU POWERED WHEELCHAIR, MODEL FC-100?

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

What is the FDA product code for FORYOU POWERED WHEELCHAIR, MODEL FC-100?

The FDA product code for FORYOU POWERED WHEELCHAIR, MODEL FC-100 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

↑