HAMILTON-MR1
K-Number: K122438 · 2013-11-20
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Device Summary
Frequently Asked Questions
What is the HAMILTON-MR1?
HAMILTON-MR1 is a medical device that received FDA 510(k) clearance on 2013-11-20. The listed applicant is Hamilton Medical AG. The 510(k) number is K122438.
When did HAMILTON-MR1 receive FDA 510(k) clearance?
HAMILTON-MR1 received FDA 510(k) clearance on 2013-11-20, under 510(k) number K122438.
Who is the listed applicant for HAMILTON-MR1?
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-MR1?
The FDA product code for HAMILTON-MR1 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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