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FDA 510(k)

SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS

K-Number: K040060 · 2004-01-28

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2004-01-28
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS 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 2004-01-28 under 510(k) number K040060. 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 SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS?

SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS is a medical device that received FDA 510(k) clearance on 2004-01-28. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K040060.

When did SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS receive FDA 510(k) clearance?

SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS received FDA 510(k) clearance on 2004-01-28, under 510(k) number K040060.

Who is the listed applicant for SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS?

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 SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS?

The FDA product code for SONOLINE G50 AND G60 S DIAGNOSTIC ULTRASOUND SYSTEMS is IYN.

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Related Devices (Code: IYN)

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.

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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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