MAGNETOM Spectra
K-Number: K153447 · 2016-03-31
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2016-03-31
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Spectra is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-03-31 under approval number K153447. 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 Spectra?
MAGNETOM Spectra is a medical device that received FDA 510(k) clearance on 2016-03-31. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K153447.
When was MAGNETOM Spectra approved by the FDA?
MAGNETOM Spectra received FDA 510(k) clearance on 2016-03-31, under approval number K153447.
What company makes MAGNETOM Spectra?
MAGNETOM Spectra is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Spectra?
The FDA product code for MAGNETOM Spectra 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.