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FDA 510(k)

Hamilton-G5

K-Number: K193228 · 2020-05-04

Decision Date2020-05-04
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Hamilton-G5 is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Medical AG. It received FDA 510(k) clearance on 2020-05-04 under 510(k) number K193228. 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-G5?

Hamilton-G5 is a medical device that received FDA 510(k) clearance on 2020-05-04. The listed applicant is Hamilton Medical AG. The 510(k) number is K193228.

When did Hamilton-G5 receive FDA 510(k) clearance?

Hamilton-G5 received FDA 510(k) clearance on 2020-05-04, under 510(k) number K193228.

Who is the listed applicant for Hamilton-G5?

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-G5?

The FDA product code for Hamilton-G5 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.

View all 9 devices →

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.