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FDA 510(k)

SYNGO MBF

K-Number: K110494 · 2011-04-06

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2011-04-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO MBF is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2011-04-06 under 510(k) number K110494. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNGO MBF?

SYNGO MBF is a medical device that received FDA 510(k) clearance on 2011-04-06. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K110494.

When did SYNGO MBF receive FDA 510(k) clearance?

SYNGO MBF received FDA 510(k) clearance on 2011-04-06, under 510(k) number K110494.

Who is the listed applicant for SYNGO MBF?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNGO MBF?

The FDA product code for SYNGO MBF is LLZ.

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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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