CUSTODIOL HTK SOLUTION
K-Number: K020924 · 2003-01-06
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Device Summary
Frequently Asked Questions
What is the CUSTODIOL HTK SOLUTION?
CUSTODIOL HTK SOLUTION is a medical device that received FDA 510(k) clearance on 2003-01-06. The listed applicant is Dr. Franz Kohler Chemie GmbH. The 510(k) number is K020924.
When did CUSTODIOL HTK SOLUTION receive FDA 510(k) clearance?
CUSTODIOL HTK SOLUTION received FDA 510(k) clearance on 2003-01-06, under 510(k) number K020924.
Who is the listed applicant for CUSTODIOL HTK SOLUTION?
The FDA 510(k) record lists Dr. Franz Kohler Chemie GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUSTODIOL HTK SOLUTION?
The FDA product code for CUSTODIOL HTK SOLUTION is KDL.
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 Dr. Franz Kohler Chemie 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: KDL)
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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