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FDA 510(k)

SIEMENS SONOLINE 4XX

K-Number: K946179 · 1995-10-03

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-10-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS SONOLINE 4XX 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 1995-10-03 under 510(k) number K946179. 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 SIEMENS SONOLINE 4XX?

SIEMENS SONOLINE 4XX is a medical device that received FDA 510(k) clearance on 1995-10-03. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K946179.

When did SIEMENS SONOLINE 4XX receive FDA 510(k) clearance?

SIEMENS SONOLINE 4XX received FDA 510(k) clearance on 1995-10-03, under 510(k) number K946179.

Who is the listed applicant for SIEMENS SONOLINE 4XX?

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 SIEMENS SONOLINE 4XX?

The FDA product code for SIEMENS SONOLINE 4XX 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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