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FDA 510(k)

AutoContour (Model RADAC V4)

K-Number: K242729 · 2024-12-09

Decision Date2024-12-09
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AutoContour (Model RADAC V4) is the device name listed in this FDA 510(k) record. The listed applicant is Radformation, Inc.. It received FDA 510(k) clearance on 2024-12-09 under 510(k) 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. The listed applicant is Radformation, Inc.. The 510(k) number is K242729.

When did AutoContour (Model RADAC V4) receive FDA 510(k) clearance?

AutoContour (Model RADAC V4) received FDA 510(k) clearance on 2024-12-09, under 510(k) number K242729.

Who is the listed applicant for AutoContour (Model RADAC V4)?

The FDA 510(k) record lists Radformation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AutoContour (Model RADAC V4)?

The FDA product code for AutoContour (Model RADAC V4) is QKB.

Other records listing Radformation, Inc. 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 16 devices →

Related Devices (Code: QKB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.