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FDA 510(k)

MAGNETOM Vida with Compressed Sensing GRASP-VIBE

K-Number: K173617 · 2018-03-30

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2018-03-30
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM Vida with Compressed Sensing GRASP-VIBE is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2018-03-30 under approval number K173617. 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 Vida with Compressed Sensing GRASP-VIBE?

MAGNETOM Vida with Compressed Sensing GRASP-VIBE is a medical device that received FDA 510(k) clearance on 2018-03-30. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K173617.

When was MAGNETOM Vida with Compressed Sensing GRASP-VIBE approved by the FDA?

MAGNETOM Vida with Compressed Sensing GRASP-VIBE received FDA 510(k) clearance on 2018-03-30, under approval number K173617.

What company makes MAGNETOM Vida with Compressed Sensing GRASP-VIBE?

MAGNETOM Vida with Compressed Sensing GRASP-VIBE is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for MAGNETOM Vida with Compressed Sensing GRASP-VIBE?

The FDA product code for MAGNETOM Vida with Compressed Sensing GRASP-VIBE 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.

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