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FDA 510(k)

ACUSON S2000 AND S3000

K-Number: K130881 · 2013-10-11

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2013-10-11
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACUSON S2000 AND S3000 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 2013-10-11 under 510(k) number K130881. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUSON S2000 AND S3000?

ACUSON S2000 AND S3000 is a medical device that received FDA 510(k) clearance on 2013-10-11. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K130881.

When did ACUSON S2000 AND S3000 receive FDA 510(k) clearance?

ACUSON S2000 AND S3000 received FDA 510(k) clearance on 2013-10-11, under 510(k) number K130881.

Who is the listed applicant for ACUSON S2000 AND S3000?

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 ACUSON S2000 AND S3000?

The FDA product code for ACUSON S2000 AND S3000 is IYN.

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Related Devices (Code: IYN)

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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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