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FDA 510(k)

SKIPPI POWERED WHEELCHAIR FOR CHILDREN

K-Number: K070318 · 2007-05-11

ApplicantOtto Bock Healthcare LP
Decision Date2007-05-11
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SKIPPI POWERED WHEELCHAIR FOR CHILDREN is the device name listed in this FDA 510(k) record. The listed applicant is Otto Bock Healthcare LP. It received FDA 510(k) clearance on 2007-05-11 under 510(k) number K070318. 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 SKIPPI POWERED WHEELCHAIR FOR CHILDREN?

SKIPPI POWERED WHEELCHAIR FOR CHILDREN is a medical device that received FDA 510(k) clearance on 2007-05-11. The listed applicant is Otto Bock Healthcare LP. The 510(k) number is K070318.

When did SKIPPI POWERED WHEELCHAIR FOR CHILDREN receive FDA 510(k) clearance?

SKIPPI POWERED WHEELCHAIR FOR CHILDREN received FDA 510(k) clearance on 2007-05-11, under 510(k) number K070318.

Who is the listed applicant for SKIPPI POWERED WHEELCHAIR FOR CHILDREN?

The FDA 510(k) record lists Otto Bock Healthcare LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKIPPI POWERED WHEELCHAIR FOR CHILDREN?

The FDA product code for SKIPPI POWERED WHEELCHAIR FOR CHILDREN is ITI.

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Other records listing Otto Bock Healthcare LP as applicant

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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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