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FDA 510(k)

SYNGO.VIA WEB VIEWER

K-Number: K111079 · 2011-05-13

ApplicantSiemens AG Medical Solutions
Decision Date2011-05-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO.VIA WEB VIEWER 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 2011-05-13 under 510(k) number K111079. 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.VIA WEB VIEWER?

SYNGO.VIA WEB VIEWER is a medical device that received FDA 510(k) clearance on 2011-05-13. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K111079.

When did SYNGO.VIA WEB VIEWER receive FDA 510(k) clearance?

SYNGO.VIA WEB VIEWER received FDA 510(k) clearance on 2011-05-13, under 510(k) number K111079.

Who is the listed applicant for SYNGO.VIA WEB VIEWER?

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.VIA WEB VIEWER?

The FDA product code for SYNGO.VIA WEB VIEWER 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.

K123920SYNGO.VIAK120331SYNGO CT DYNAMIC ANGIOK101666SYNGO. PLAZA VA20AK100637SYNGO.CT CORONARY ANALYSISK093612SYNGO.PLAZAK092067ABVS WORKPLACE

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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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