CHROMOPHARE X 65
K-Number: K024132 · 2003-03-21
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Device Summary
Frequently Asked Questions
What is the CHROMOPHARE X 65?
CHROMOPHARE X 65 is a medical device that received FDA 510(k) clearance on 2003-03-21. The listed applicant is Berchtold Holding GmbH. The 510(k) number is K024132.
When did CHROMOPHARE X 65 receive FDA 510(k) clearance?
CHROMOPHARE X 65 received FDA 510(k) clearance on 2003-03-21, under 510(k) number K024132.
Who is the listed applicant for CHROMOPHARE X 65?
The FDA 510(k) record lists Berchtold Holding GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHROMOPHARE X 65?
The FDA product code for CHROMOPHARE X 65 is FSY.
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 Berchtold Holding GmbH 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: FSY)
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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