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FDA 510(k)

E Z CHAIR

K-Number: K993298 · 1999-11-16

Decision Date1999-11-16
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

E Z CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Premier Designs. It received FDA 510(k) clearance on 1999-11-16 under 510(k) number K993298. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E Z CHAIR?

E Z CHAIR is a medical device that received FDA 510(k) clearance on 1999-11-16. The listed applicant is Premier Designs. The 510(k) number is K993298.

When did E Z CHAIR receive FDA 510(k) clearance?

E Z CHAIR received FDA 510(k) clearance on 1999-11-16, under 510(k) number K993298.

Who is the listed applicant for E Z CHAIR?

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

What is the FDA product code for E Z CHAIR?

The FDA product code for E Z CHAIR is IOR.

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: IOR)

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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