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FDA 510(k)

SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS

K-Number: K042833 · 2004-10-27

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2004-10-27
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOLINE G20 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 2004-10-27 under 510(k) number K042833. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS?

SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS is a medical device that received FDA 510(k) clearance on 2004-10-27. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K042833.

When did SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS receive FDA 510(k) clearance?

SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS received FDA 510(k) clearance on 2004-10-27, under 510(k) number K042833.

Who is the listed applicant for SONOLINE G20 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 G20 DIAGNOSTIC ULTRASOUND SYSTEMS?

The FDA product code for SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS is IYO.

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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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