HAMILTON-C3
K-Number: K123637 · 2012-12-21
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Device Summary
Frequently Asked Questions
What is the HAMILTON-C3?
HAMILTON-C3 is a medical device that received FDA 510(k) clearance on 2012-12-21. The listed applicant is Hamilton Medical AG. The 510(k) number is K123637.
When did HAMILTON-C3 receive FDA 510(k) clearance?
HAMILTON-C3 received FDA 510(k) clearance on 2012-12-21, under 510(k) number K123637.
Who is the listed applicant for HAMILTON-C3?
The FDA 510(k) record lists Hamilton Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HAMILTON-C3?
The FDA product code for HAMILTON-C3 is CBK.
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 Hamilton Medical AG 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: CBK)
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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