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FDA 510(k)

ETIAM STAR PACS COMPONENTS

K-Number: K052358 · 2005-10-05

ApplicantEtiam, S.A.
Decision Date2005-10-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ETIAM STAR PACS COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is Etiam, S.A.. It received FDA 510(k) clearance on 2005-10-05 under 510(k) number K052358. 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 ETIAM STAR PACS COMPONENTS?

ETIAM STAR PACS COMPONENTS is a medical device that received FDA 510(k) clearance on 2005-10-05. The listed applicant is Etiam, S.A.. The 510(k) number is K052358.

When did ETIAM STAR PACS COMPONENTS receive FDA 510(k) clearance?

ETIAM STAR PACS COMPONENTS received FDA 510(k) clearance on 2005-10-05, under 510(k) number K052358.

Who is the listed applicant for ETIAM STAR PACS COMPONENTS?

The FDA 510(k) record lists Etiam, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETIAM STAR PACS COMPONENTS?

The FDA product code for ETIAM STAR PACS COMPONENTS is LLZ.

Related Clinical Trials

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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