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FDA 510(k)

ZIPPY

K-Number: K983808 · 1999-10-14

ApplicantPillar Technology, Inc.
Decision Date1999-10-14
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ZIPPY is the device name listed in this FDA 510(k) record. The listed applicant is Pillar Technology, Inc.. It received FDA 510(k) clearance on 1999-10-14 under 510(k) number K983808. 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 ZIPPY?

ZIPPY is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Pillar Technology, Inc.. The 510(k) number is K983808.

When did ZIPPY receive FDA 510(k) clearance?

ZIPPY received FDA 510(k) clearance on 1999-10-14, under 510(k) number K983808.

Who is the listed applicant for ZIPPY?

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

What is the FDA product code for ZIPPY?

The FDA product code for ZIPPY 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 Pillar Technology, 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.

K012846ZIPPY, MODEL I88WAK994127GLORYK972851ZIPPYK961888PILLAR 4-WHEEL SCOOTERK910265TRAVELER, MOTORIZED THREE-WHEELED VEHICLE

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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