HAMILTON-C3
K-Number: K161450 · 2017-04-27
Device Summary
Frequently Asked Questions
What is the HAMILTON-C3?
HAMILTON-C3 is a medical device that received FDA 510(k) clearance on 2017-04-27. The listed applicant is Hamilton Medical AG. The 510(k) number is K161450.
When did HAMILTON-C3 receive FDA 510(k) clearance?
HAMILTON-C3 received FDA 510(k) clearance on 2017-04-27, under 510(k) number K161450.
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.
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.