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FDA 510(k)

SHOWCASE

K-Number: K082135 · 2008-10-21

ApplicantTrillium Technology, Inc.
Decision Date2008-10-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHOWCASE is the device name listed in this FDA 510(k) record. The listed applicant is Trillium Technology, Inc.. It received FDA 510(k) clearance on 2008-10-21 under 510(k) number K082135. 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 SHOWCASE?

SHOWCASE is a medical device that received FDA 510(k) clearance on 2008-10-21. The listed applicant is Trillium Technology, Inc.. The 510(k) number is K082135.

When did SHOWCASE receive FDA 510(k) clearance?

SHOWCASE received FDA 510(k) clearance on 2008-10-21, under 510(k) number K082135.

Who is the listed applicant for SHOWCASE?

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

What is the FDA product code for SHOWCASE?

The FDA product code for SHOWCASE is LLZ.

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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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