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FDA 510(k)

JYROCHAIR POWER WHEELCHAIR

K-Number: K900514 · 1990-02-27

Decision Date1990-02-27
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JYROCHAIR POWER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Jyrochair, Inc.. It received FDA 510(k) clearance on 1990-02-27 under 510(k) number K900514. 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 JYROCHAIR POWER WHEELCHAIR?

JYROCHAIR POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Jyrochair, Inc.. The 510(k) number is K900514.

When did JYROCHAIR POWER WHEELCHAIR receive FDA 510(k) clearance?

JYROCHAIR POWER WHEELCHAIR received FDA 510(k) clearance on 1990-02-27, under 510(k) number K900514.

Who is the listed applicant for JYROCHAIR POWER WHEELCHAIR?

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

What is the FDA product code for JYROCHAIR POWER WHEELCHAIR?

The FDA product code for JYROCHAIR POWER WHEELCHAIR 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.

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.

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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