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FDA 510(k)

ZIPPY, MODEL I88WA

K-Number: K012846 · 2001-11-20

ApplicantPillar Technology, Inc.
Decision Date2001-11-20
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ZIPPY, MODEL I88WA 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 2001-11-20 under 510(k) number K012846. 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, MODEL I88WA?

ZIPPY, MODEL I88WA is a medical device that received FDA 510(k) clearance on 2001-11-20. The listed applicant is Pillar Technology, Inc.. The 510(k) number is K012846.

When did ZIPPY, MODEL I88WA receive FDA 510(k) clearance?

ZIPPY, MODEL I88WA received FDA 510(k) clearance on 2001-11-20, under 510(k) number K012846.

Who is the listed applicant for ZIPPY, MODEL I88WA?

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, MODEL I88WA?

The FDA product code for ZIPPY, MODEL I88WA is ITI.

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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.

K994127GLORYK983808ZIPPYK972851ZIPPYK961888PILLAR 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.

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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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