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FDA 510(k)

KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM

K-Number: K023772 · 2002-11-22

ApplicantAcuson Corp.
Decision Date2002-11-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 2002-11-22 under 510(k) number K023772. 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 KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM?

KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-22. The listed applicant is Acuson Corp.. The 510(k) number is K023772.

When did KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM receive FDA 510(k) clearance?

KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM received FDA 510(k) clearance on 2002-11-22, under 510(k) number K023772.

Who is the listed applicant for KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM?

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 KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM?

The FDA product code for KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM 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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