MAGNETOM Sola; MAGNETOM Altea
K-Number: K232535 · 2023-12-22
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2023-12-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Sola; MAGNETOM Altea is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2023-12-22 under approval number K232535. 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 MAGNETOM Sola; MAGNETOM Altea?
MAGNETOM Sola; MAGNETOM Altea is a medical device that received FDA 510(k) clearance on 2023-12-22. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K232535.
When was MAGNETOM Sola; MAGNETOM Altea approved by the FDA?
MAGNETOM Sola; MAGNETOM Altea received FDA 510(k) clearance on 2023-12-22, under approval number K232535.
What company makes MAGNETOM Sola; MAGNETOM Altea?
MAGNETOM Sola; MAGNETOM Altea is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Sola; MAGNETOM Altea?
The FDA product code for MAGNETOM Sola; MAGNETOM Altea 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.