Visible Patient Suite— 510(k) K151988

Name: FDA 510(k) clearance K151988
Creator: U.S. Food and Drug Administration
Published: 2015-10-15

Substantially Equivalent

Visible Patient, Sas

FDA 510(k) clearance K151988 for Visible Patient Suite, Substantially Equivalent on 2015-10-15. Applicant: Visible Patient, Sas. Device class: 2.

Clearance details

Applicant: Visible Patient, Sas
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2015-07-17
Decision date: 2015-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Strasbourg, FR

Download summary PDF View on FDA.gov ↗

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K212896 — Visible Patient Suite2021-11-05

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.