COLORISE RIGID
K-Number: K081084 · 2008-05-14
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Device Summary
Frequently Asked Questions
What is the COLORISE RIGID?
COLORISE RIGID is a medical device that received FDA 510(k) clearance on 2008-05-14. The listed applicant is Zhermack S.P.A.. The 510(k) number is K081084.
When did COLORISE RIGID receive FDA 510(k) clearance?
COLORISE RIGID received FDA 510(k) clearance on 2008-05-14, under 510(k) number K081084.
Who is the listed applicant for COLORISE RIGID?
The FDA 510(k) record lists Zhermack S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLORISE RIGID?
The FDA product code for COLORISE RIGID is ELW.
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 Zhermack S.P.A. 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: ELW)
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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