SILHOUETTE VR— 510(k) K982955

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K982955 for SILHOUETTE VR, Substantially Equivalent on 1998-11-04. Applicant: GE Medical Systems.

Clearance details

Applicant: GE Medical Systems
Product code: Code KPR
Advisory panel: Radiology
Date received: 1998-08-24
Decision date: 1998-11-04
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.