AutoContour (Model RADAC V4)
K-Number: K242729 · 2024-12-09
ApplicantRadformation, Inc.
Decision Date2024-12-09
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
AutoContour (Model RADAC V4) is a medical device manufactured by Radformation, Inc.. It received FDA 510(k) clearance on 2024-12-09 under approval number K242729. 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 V4)?
AutoContour (Model RADAC V4) is a medical device that received FDA 510(k) clearance on 2024-12-09. It is manufactured by Radformation, Inc.. The 510(k) number is K242729.
When was AutoContour (Model RADAC V4) approved by the FDA?
AutoContour (Model RADAC V4) received FDA 510(k) clearance on 2024-12-09, under approval number K242729.
What company makes AutoContour (Model RADAC V4)?
AutoContour (Model RADAC V4) is manufactured by Radformation, Inc..
What is the FDA product code for AutoContour (Model RADAC V4)?
The FDA product code for AutoContour (Model RADAC V4) 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.