MAGNETOM Lumina
K-Number: K183244 · 2019-01-24
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2019-01-24
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MAGNETOM Lumina is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2019-01-24 under approval number K183244. 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 Lumina?
MAGNETOM Lumina is a medical device that received FDA 510(k) clearance on 2019-01-24. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K183244.
When was MAGNETOM Lumina approved by the FDA?
MAGNETOM Lumina received FDA 510(k) clearance on 2019-01-24, under approval number K183244.
What company makes MAGNETOM Lumina?
MAGNETOM Lumina is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for MAGNETOM Lumina?
The FDA product code for MAGNETOM Lumina is LNH.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: LNH)
K162940MultiBand SENSEPhilips Medical Systems Nederland B.V.
K162183Vantage Galan 3T, MRT-3020, V4.0Toshibamedical Systems Corporation
K162102MAGNETOM Avantofit, MAGNETOM SkyrafitSiemens Medi Cal Solutions, Inc.
K162403HyperBandGe Medical Systems, LLC
K161795MAGNETOM ESSENZASiemens Medical Solutions USA, Inc.
K161973G-scan Brio, S-scanEsaote, S.p.A.
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.