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FDA 510(k)

SYNGO.VIA

K-Number: K123375 · 2012-11-20

ApplicantSiemens AG
Decision Date2012-11-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO.VIA is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG. It received FDA 510(k) clearance on 2012-11-20 under 510(k) number K123375. 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?

SYNGO.VIA is a medical device that received FDA 510(k) clearance on 2012-11-20. The listed applicant is Siemens AG. The 510(k) number is K123375.

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

SYNGO.VIA received FDA 510(k) clearance on 2012-11-20, under 510(k) number K123375.

Who is the listed applicant for SYNGO.VIA?

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

What is the FDA product code for SYNGO.VIA?

The FDA product code for SYNGO.VIA is LLZ.

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Other records listing Siemens AG 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.

K110366SYNGO.CT CARDIAC FUNCTIONK071310SYNGO CT ONCOLOGY SOFTWARE PACKAGEK063507SYNGO NEURO PBV CTK063373FLEX LOOP COIL SET 3TK053024SYNGO NEURO DSA CTK050867SYNGO BODY PERFUSION-CT

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Related Devices (Code: 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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