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FDA 510(k)

CSV12 SOFTWARE VIEWER

K-Number: K022896 · 2002-10-03

ApplicantAcuson Corp.
Decision Date2002-10-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CSV12 SOFTWARE VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 2002-10-03 under 510(k) number K022896. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CSV12 SOFTWARE VIEWER?

CSV12 SOFTWARE VIEWER is a medical device that received FDA 510(k) clearance on 2002-10-03. The listed applicant is Acuson Corp.. The 510(k) number is K022896.

When did CSV12 SOFTWARE VIEWER receive FDA 510(k) clearance?

CSV12 SOFTWARE VIEWER received FDA 510(k) clearance on 2002-10-03, under 510(k) number K022896.

Who is the listed applicant for CSV12 SOFTWARE VIEWER?

The FDA 510(k) record lists Acuson Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CSV12 SOFTWARE VIEWER?

The FDA product code for CSV12 SOFTWARE VIEWER is LLZ.

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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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