MAGNETOM Sola
K-Number: K182129 · 2018-10-12
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2018-10-12
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Sola is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2018-10-12 under approval number K182129. 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 Sola is a medical device that received FDA 510(k) clearance on 2018-10-12. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K182129.
When was MAGNETOM Sola approved by the FDA?
MAGNETOM Sola received FDA 510(k) clearance on 2018-10-12, under approval number K182129.
What company makes MAGNETOM Sola?
MAGNETOM Sola is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Sola?
The FDA product code for MAGNETOM Sola 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.