IMLOGIX 1000 IMAGE DISPLAY SYSTEM— 510(k) K893521

Substantially Equivalent

Imlogix A Div. of Microterm

FDA 510(k) clearance K893521 for IMLOGIX 1000 IMAGE DISPLAY SYSTEM, Substantially Equivalent on 1989-06-23. Applicant: Imlogix A Div. of Microterm.

Clearance details

Applicant: Imlogix A Div. of Microterm
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1989-05-08
Decision date: 1989-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.