SOLARIX FV— 510(k) K953832

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K953832 for SOLARIX FV, Substantially Equivalent on 1995-09-12. Applicant: GE Medical Systems.

Clearance details

Applicant: GE Medical Systems
Product code: Code KPR
Advisory panel: Radiology
Date received: 1995-08-16
Decision date: 1995-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

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Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.