SHOWCASE

System, Image Processing, Radiological

TRILLIUM TECHNOLOGY, INC

The following data is part of a premarket notification filed by Trillium Technology, Inc with the FDA for Showcase.

Pre-market Notification Details

• Device ID: K082135
• 510k Number: K082135
• Device Name: SHOWCASE
• Classification: System, Image Processing, Radiological
• Applicant: TRILLIUM TECHNOLOGY, INC 16303 PANORAMIC WAY San Leandro, CA 94578 -1116
• Contact: Gary J Allsebrook
• Correspondent: Gary J Allsebrook; TRILLIUM TECHNOLOGY, INC 16303 PANORAMIC WAY San Leandro, CA 94578 -1116
• Product Code: LLZ
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2008-07-29
• Decision Date: 2008-10-21
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00865885000206	K082135	000