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FDA 510(k)

SONOLINE SX ULTRASOUND SCANNER

K-Number: K852739 · 1986-03-10

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1986-03-10
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SONOLINE SX ULTRASOUND SCANNER 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 1986-03-10 under 510(k) number K852739. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOLINE SX ULTRASOUND SCANNER?

SONOLINE SX ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1986-03-10. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K852739.

When did SONOLINE SX ULTRASOUND SCANNER receive FDA 510(k) clearance?

SONOLINE SX ULTRASOUND SCANNER received FDA 510(k) clearance on 1986-03-10, under 510(k) number K852739.

Who is the listed applicant for SONOLINE SX ULTRASOUND SCANNER?

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 SX ULTRASOUND SCANNER?

The FDA product code for SONOLINE SX ULTRASOUND SCANNER is DXK.

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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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