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FDA 510(k)

QUICKIE POWER WHEELCHAIRS P200 SERIES

K-Number: K963385 · 1997-04-28

ApplicantQuickie Designs, Inc.
Decision Date1997-04-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUICKIE POWER WHEELCHAIRS P200 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Quickie Designs, Inc.. It received FDA 510(k) clearance on 1997-04-28 under 510(k) number K963385. 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 QUICKIE POWER WHEELCHAIRS P200 SERIES?

QUICKIE POWER WHEELCHAIRS P200 SERIES is a medical device that received FDA 510(k) clearance on 1997-04-28. The listed applicant is Quickie Designs, Inc.. The 510(k) number is K963385.

When did QUICKIE POWER WHEELCHAIRS P200 SERIES receive FDA 510(k) clearance?

QUICKIE POWER WHEELCHAIRS P200 SERIES received FDA 510(k) clearance on 1997-04-28, under 510(k) number K963385.

Who is the listed applicant for QUICKIE POWER WHEELCHAIRS P200 SERIES?

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

What is the FDA product code for QUICKIE POWER WHEELCHAIRS P200 SERIES?

The FDA product code for QUICKIE POWER WHEELCHAIRS P200 SERIES 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

Other records listing Quickie Designs, 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.

K972230QUICKIE P90 SERIESK963382QUICKIE P100 SERIESK963381QUICKIE P300 SERIESK924278QUICKIE P200K900330QUICKIE P300 WHEELCHAIR

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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