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FDA 510(k)

CADDY

K-Number: K041186 · 2004-09-09

ApplicantAfikim Electric Vehicles
Decision Date2004-09-09
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CADDY is the device name listed in this FDA 510(k) record. The listed applicant is Afikim Electric Vehicles. It received FDA 510(k) clearance on 2004-09-09 under 510(k) number K041186. 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 CADDY?

CADDY is a medical device that received FDA 510(k) clearance on 2004-09-09. The listed applicant is Afikim Electric Vehicles. The 510(k) number is K041186.

When did CADDY receive FDA 510(k) clearance?

CADDY received FDA 510(k) clearance on 2004-09-09, under 510(k) number K041186.

Who is the listed applicant for CADDY?

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

What is the FDA product code for CADDY?

The FDA product code for CADDY is ITI.

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Other records listing Afikim Electric Vehicles 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.

K102304BREEZE C MODEL C (3W), BREEZE C (4W)K051028BREEZE

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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