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FDA 510(k)

CENTRICITY PACS PLUS

K-Number: K023557 · 2002-11-07

ApplicantGE Medical Systems
Decision Date2002-11-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CENTRICITY PACS PLUS is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 2002-11-07 under 510(k) number K023557. 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 CENTRICITY PACS PLUS?

CENTRICITY PACS PLUS is a medical device that received FDA 510(k) clearance on 2002-11-07. The listed applicant is GE Medical Systems. The 510(k) number is K023557.

When did CENTRICITY PACS PLUS receive FDA 510(k) clearance?

CENTRICITY PACS PLUS received FDA 510(k) clearance on 2002-11-07, under 510(k) number K023557.

Who is the listed applicant for CENTRICITY PACS PLUS?

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

What is the FDA product code for CENTRICITY PACS PLUS?

The FDA product code for CENTRICITY PACS PLUS is LLZ.

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Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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