SIGNA MAGNUS
K-Number: K241242 · 2024-10-17
ApplicantGe Medical Systems, LLC
Decision Date2024-10-17
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
SIGNA MAGNUS is a medical device manufactured by Ge Medical Systems, LLC. It received FDA 510(k) clearance on 2024-10-17 under approval number K241242. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SIGNA MAGNUS?
SIGNA MAGNUS is a medical device that received FDA 510(k) clearance on 2024-10-17. It is manufactured by Ge Medical Systems, LLC. The 510(k) number is K241242.
When was SIGNA MAGNUS approved by the FDA?
SIGNA MAGNUS received FDA 510(k) clearance on 2024-10-17, under approval number K241242.
What company makes SIGNA MAGNUS?
SIGNA MAGNUS is manufactured by Ge Medical Systems, LLC.
What is the FDA product code for SIGNA MAGNUS?
The FDA product code for SIGNA MAGNUS is LNH.
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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.