ANGIOTEC ZX DIGITAL IMAGE PROCESSOR— 510(k) K892869

Substantially Equivalent

Andros Analyzers, Inc.

FDA 510(k) clearance K892869 for ANGIOTEC ZX DIGITAL IMAGE PROCESSOR, Substantially Equivalent on 1989-05-26. Applicant: Andros Analyzers, Inc..

Clearance details

Applicant: Andros Analyzers, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1989-04-19
Decision date: 1989-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Berkeley, CA, 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.