Auto Segmentation
K-Number: K230082 · 2023-05-04
ApplicantGe Medical Systems, LLC
Decision Date2023-05-04
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Auto Segmentation is a medical device manufactured by Ge Medical Systems, LLC. It received FDA 510(k) clearance on 2023-05-04 under approval number K230082. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Auto Segmentation?
Auto Segmentation is a medical device that received FDA 510(k) clearance on 2023-05-04. It is manufactured by Ge Medical Systems, LLC. The 510(k) number is K230082.
When was Auto Segmentation approved by the FDA?
Auto Segmentation received FDA 510(k) clearance on 2023-05-04, under approval number K230082.
What company makes Auto Segmentation?
Auto Segmentation is manufactured by Ge Medical Systems, LLC.
What is the FDA product code for Auto Segmentation?
The FDA product code for Auto Segmentation is QKB.
Other Devices by Ge Medical Systems, LLC
Related Devices (Code: QKB)
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.