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FDA 510(k)

ALZ WEB PACS, VERSION 1.0

K-Number: K081304 · 2008-06-11

ApplicantAlz, Inc.
Decision Date2008-06-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALZ WEB PACS, VERSION 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Alz, Inc.. It received FDA 510(k) clearance on 2008-06-11 under 510(k) number K081304. 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 ALZ WEB PACS, VERSION 1.0?

ALZ WEB PACS, VERSION 1.0 is a medical device that received FDA 510(k) clearance on 2008-06-11. The listed applicant is Alz, Inc.. The 510(k) number is K081304.

When did ALZ WEB PACS, VERSION 1.0 receive FDA 510(k) clearance?

ALZ WEB PACS, VERSION 1.0 received FDA 510(k) clearance on 2008-06-11, under 510(k) number K081304.

Who is the listed applicant for ALZ WEB PACS, VERSION 1.0?

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

What is the FDA product code for ALZ WEB PACS, VERSION 1.0?

The FDA product code for ALZ WEB PACS, VERSION 1.0 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

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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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