MR Contour DL
K-Number: K242925 · 2025-04-01
ApplicantGE Healthcare
Decision Date2025-04-01
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MR Contour DL is a medical device manufactured by GE Healthcare. It received FDA 510(k) clearance on 2025-04-01 under approval number K242925. 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 MR Contour DL?
MR Contour DL is a medical device that received FDA 510(k) clearance on 2025-04-01. It is manufactured by GE Healthcare. The 510(k) number is K242925.
When was MR Contour DL approved by the FDA?
MR Contour DL received FDA 510(k) clearance on 2025-04-01, under approval number K242925.
What company makes MR Contour DL?
MR Contour DL is manufactured by GE Healthcare.
What is the FDA product code for MR Contour DL?
The FDA product code for MR Contour DL is QKB.
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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.