FDA 510(k)

SONOLINE CF

K-Number: K875272 · 1988-02-18

ApplicantSiemens Medical Laboratories, Inc.

Decision Date1988-02-18

Product CodeDXK

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SONOLINE CF is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K875272. 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 CF?

SONOLINE CF is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Siemens Medical Laboratories, Inc.. The 510(k) number is K875272.

When did SONOLINE CF receive FDA 510(k) clearance?

SONOLINE CF received FDA 510(k) clearance on 1988-02-18, under 510(k) number K875272.

Who is the listed applicant for SONOLINE CF?

The FDA 510(k) record lists Siemens Medical Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONOLINE CF?

The FDA product code for SONOLINE CF is DXK.

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Other records listing Siemens Medical Laboratories, Inc. as applicant

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Related Devices (Code: 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.