COLORBITE
K-Number: K053619 · 2006-03-01
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Device Summary
Frequently Asked Questions
What is the COLORBITE?
COLORBITE is a medical device that received FDA 510(k) clearance on 2006-03-01. The listed applicant is Zhermack S.P.A.. The 510(k) number is K053619.
When did COLORBITE receive FDA 510(k) clearance?
COLORBITE received FDA 510(k) clearance on 2006-03-01, under 510(k) number K053619.
Who is the listed applicant for COLORBITE?
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 COLORBITE?
The FDA product code for COLORBITE 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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