AutoContour Model RADAC V3
K-Number: K230685 · 2023-04-14
ApplicantRadformation, Inc.
Decision Date2023-04-14
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
AutoContour Model RADAC V3 is a medical device manufactured by Radformation, Inc.. It received FDA 510(k) clearance on 2023-04-14 under approval number K230685. 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 AutoContour Model RADAC V3?
AutoContour Model RADAC V3 is a medical device that received FDA 510(k) clearance on 2023-04-14. It is manufactured by Radformation, Inc.. The 510(k) number is K230685.
When was AutoContour Model RADAC V3 approved by the FDA?
AutoContour Model RADAC V3 received FDA 510(k) clearance on 2023-04-14, under approval number K230685.
What company makes AutoContour Model RADAC V3?
AutoContour Model RADAC V3 is manufactured by Radformation, Inc..
What is the FDA product code for AutoContour Model RADAC V3?
The FDA product code for AutoContour Model RADAC V3 is QKB.
Other Devices by Radformation, Inc.
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.