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FDA 510(k)

QUICKIE P200

K-Number: K924278 · 1994-03-28

ApplicantQuickie Designs, Inc.
Decision Date1994-03-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

QUICKIE P200 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 1994-03-28 under 510(k) number K924278. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the QUICKIE P200?

QUICKIE P200 is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Quickie Designs, Inc.. The 510(k) number is K924278.

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

QUICKIE P200 received FDA 510(k) clearance on 1994-03-28, under 510(k) number K924278.

Who is the listed applicant for QUICKIE P200?

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 P200?

The FDA product code for QUICKIE P200 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.

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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 SERIESK963385QUICKIE POWER WHEELCHAIRS P200 SERIESK963381QUICKIE P300 SERIESK900330QUICKIE 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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