VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM— 510(k) K900064

Name: FDA 510(k) clearance K900064
Creator: U.S. Food and Drug Administration
Published: 1990-03-09

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K900064 for VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM, Substantially Equivalent on 1990-03-09. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code LNH
Device class: Class 2
Regulation: 21 CFR 892.1000
Advisory panel: Radiology
Date received: 1990-01-04
Decision date: 1990-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LNH

product code LNH

Death: 11
Injury: 670
Malfunction: 1,460
Other: 2
Total: 2,143

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.