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FDA 510(k)

syngo.via View&GO (Version VA10A)

K-Number: K182208 · 2018-09-07

ApplicantSiemens Healthcare GmbH
Decision Date2018-09-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo.via View&GO (Version VA10A) is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2018-09-07 under 510(k) number K182208. 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 View&GO (Version VA10A)?

syngo.via View&GO (Version VA10A) is a medical device that received FDA 510(k) clearance on 2018-09-07. The listed applicant is Siemens Healthcare GmbH. The 510(k) number is K182208.

When did syngo.via View&GO (Version VA10A) receive FDA 510(k) clearance?

syngo.via View&GO (Version VA10A) received FDA 510(k) clearance on 2018-09-07, under 510(k) number K182208.

Who is the listed applicant for syngo.via View&GO (Version VA10A)?

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

What is the FDA product code for syngo.via View&GO (Version VA10A)?

The FDA product code for syngo.via View&GO (Version VA10A) 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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