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FDA 510(k)

SYNGO LUNG CAD

K-Number: K063877 · 2006-10-18

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2006-10-18
Product CodeOEB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO LUNG CAD is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2006-10-18 under 510(k) number K063877. The device is classified under product code OEB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNGO LUNG CAD?

SYNGO LUNG CAD is a medical device that received FDA 510(k) clearance on 2006-10-18. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K063877.

When did SYNGO LUNG CAD receive FDA 510(k) clearance?

SYNGO LUNG CAD received FDA 510(k) clearance on 2006-10-18, under 510(k) number K063877.

Who is the listed applicant for SYNGO LUNG CAD?

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

What is the FDA product code for SYNGO LUNG CAD?

The FDA product code for SYNGO LUNG CAD is OEB.

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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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