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FDA 510(k)

EUROCHAIR

K-Number: K050560 · 2005-04-21

ApplicantMeyra, Inc.
Decision Date2005-04-21
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EUROCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Meyra, Inc.. It received FDA 510(k) clearance on 2005-04-21 under 510(k) number K050560. 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 EUROCHAIR?

EUROCHAIR is a medical device that received FDA 510(k) clearance on 2005-04-21. The listed applicant is Meyra, Inc.. The 510(k) number is K050560.

When did EUROCHAIR receive FDA 510(k) clearance?

EUROCHAIR received FDA 510(k) clearance on 2005-04-21, under 510(k) number K050560.

Who is the listed applicant for EUROCHAIR?

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

What is the FDA product code for EUROCHAIR?

The FDA product code for EUROCHAIR 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.

Other records listing Meyra, 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.

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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