PRESTILIX 1694 D IMAGE INTENSIFIED FLUOROSCCOPIC— 510(k) K924310

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K924310 for PRESTILIX 1694 D IMAGE INTENSIFIED FLUOROSCCOPIC, Substantially Equivalent on 1993-01-21. Applicant: GE Medical Systems.

Clearance details

Applicant: GE Medical Systems
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1992-08-26
Decision date: 1993-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, 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.