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FDA 510(k)

SONOLINE 3000

K-Number: K827455 · 1982-07-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1982-07-07
Product Code
DecisionSubstantially Equivalent

Device Summary

SONOLINE 3000 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 1982-07-07 under 510(k) number K827455. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOLINE 3000?

SONOLINE 3000 is a medical device that received FDA 510(k) clearance on 1982-07-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K827455.

When did SONOLINE 3000 receive FDA 510(k) clearance?

SONOLINE 3000 received FDA 510(k) clearance on 1982-07-07, under 510(k) number K827455.

Who is the listed applicant for SONOLINE 3000?

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

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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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