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FDA 510(k)

HITCH HIKER

K-Number: K823117 · 1982-11-16

ApplicantAmigo Sales, Inc.
Decision Date1982-11-16
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HITCH HIKER is the device name listed in this FDA 510(k) record. The listed applicant is Amigo Sales, Inc.. It received FDA 510(k) clearance on 1982-11-16 under 510(k) number K823117. 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 HITCH HIKER?

HITCH HIKER is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Amigo Sales, Inc.. The 510(k) number is K823117.

When did HITCH HIKER receive FDA 510(k) clearance?

HITCH HIKER received FDA 510(k) clearance on 1982-11-16, under 510(k) number K823117.

Who is the listed applicant for HITCH HIKER?

The FDA 510(k) record lists Amigo Sales, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HITCH HIKER?

The FDA product code for HITCH HIKER is ITI.

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Other records listing Amigo Sales, Inc. 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.

K871391AMIGO-A288310 (SCOOTER, COMMUTER CART, 3-WHEELED)K853918THE SPORTSTER (ELECTRIFIED WHEELCHAIR)K852557ALL TERRAIN AMIGOK830345SCOOTER, VEHICLE MOTORIZEDK820858ESCORTK800209BOOTS - OUTDOOR CARRIER FOR THE AMIGO

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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.

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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