SIGNA Victor
K-Number: K223439 · 2023-02-13
Decision Date2023-02-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
SIGNA Victor is a medical device manufactured by Ge Healthcare (Tianjin) Company Limited. It received FDA 510(k) clearance on 2023-02-13 under approval number K223439. 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 Victor?
SIGNA Victor is a medical device that received FDA 510(k) clearance on 2023-02-13. It is manufactured by Ge Healthcare (Tianjin) Company Limited. The 510(k) number is K223439.
When was SIGNA Victor approved by the FDA?
SIGNA Victor received FDA 510(k) clearance on 2023-02-13, under approval number K223439.
What company makes SIGNA Victor?
SIGNA Victor is manufactured by Ge Healthcare (Tianjin) Company Limited.
What is the FDA product code for SIGNA Victor?
The FDA product code for SIGNA Victor 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.