HAMILTON-C3
K-Number: K161450 · 2017-04-27
ApplicantHamilton Medical AG
Decision Date2017-04-27
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
HAMILTON-C3 is a medical device manufactured by Hamilton Medical AG. It received FDA 510(k) clearance on 2017-04-27 under approval number K161450. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the HAMILTON-C3?
HAMILTON-C3 is a medical device that received FDA 510(k) clearance on 2017-04-27. It is manufactured by Hamilton Medical AG. The 510(k) number is K161450.
When was HAMILTON-C3 approved by the FDA?
HAMILTON-C3 received FDA 510(k) clearance on 2017-04-27, under approval number K161450.
What company makes HAMILTON-C3?
HAMILTON-C3 is manufactured by Hamilton Medical AG.
What is the FDA product code for HAMILTON-C3?
The FDA product code for HAMILTON-C3 is CBK.
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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.