FDA 510(k)

SYNGO MULTIMODALITY WORKPLACE (SYNGO MM WP)

K-Number: K052775 · 2005-10-31

Decision Date2005-10-31

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SYNGO MULTIMODALITY WORKPLACE (SYNGO MM WP) 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 2005-10-31 under 510(k) number K052775. 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 MM WP)?

SYNGO MULTIMODALITY WORKPLACE (SYNGO MM WP) is a medical device that received FDA 510(k) clearance on 2005-10-31. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K052775.

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

SYNGO MULTIMODALITY WORKPLACE (SYNGO MM WP) received FDA 510(k) clearance on 2005-10-31, under 510(k) number K052775.

Who is the listed applicant for SYNGO MULTIMODALITY WORKPLACE (SYNGO MM WP)?

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 (SYNGO MM WP)?

The FDA product code for SYNGO MULTIMODALITY WORKPLACE (SYNGO MM WP) is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.