EUROCHAIR
K-Number: K050560 · 2005-04-21
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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