COLORISE
K-Number: K070677 · 2007-05-11
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Device Summary
Frequently Asked Questions
What is the COLORISE?
COLORISE is a medical device that received FDA 510(k) clearance on 2007-05-11. The listed applicant is Zhermack S.P.A.. The 510(k) number is K070677.
When did COLORISE receive FDA 510(k) clearance?
COLORISE received FDA 510(k) clearance on 2007-05-11, under 510(k) number K070677.
Who is the listed applicant for COLORISE?
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?
The FDA product code for COLORISE 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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