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FDA 510(k)

SYNGO US WORKPLACE

K-Number: K091286 · 2009-05-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2009-05-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO US WORKPLACE 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 2009-05-15 under 510(k) number K091286. 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 US WORKPLACE?

SYNGO US WORKPLACE is a medical device that received FDA 510(k) clearance on 2009-05-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K091286.

When did SYNGO US WORKPLACE receive FDA 510(k) clearance?

SYNGO US WORKPLACE received FDA 510(k) clearance on 2009-05-15, under 510(k) number K091286.

Who is the listed applicant for SYNGO US WORKPLACE?

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 US WORKPLACE?

The FDA product code for SYNGO US WORKPLACE 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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