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FDA 510(k)

SYNGO MULTIMODALITY WORKPLACE

K-Number: K061964 · 2006-07-27

ApplicantSiemens AG Medical Solutions
Decision Date2006-07-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO MULTIMODALITY WORKPLACE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG Medical Solutions. It received FDA 510(k) clearance on 2006-07-27 under 510(k) number K061964. 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 MULTIMODALITY WORKPLACE?

SYNGO MULTIMODALITY WORKPLACE is a medical device that received FDA 510(k) clearance on 2006-07-27. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K061964.

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

SYNGO MULTIMODALITY WORKPLACE received FDA 510(k) clearance on 2006-07-27, under 510(k) number K061964.

Who is the listed applicant for SYNGO MULTIMODALITY WORKPLACE?

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

What is the FDA product code for SYNGO MULTIMODALITY WORKPLACE?

The FDA product code for SYNGO MULTIMODALITY WORKPLACE is LLZ.

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Other records listing Siemens AG Medical Solutions as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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