VISTA MR 2055 HP SYSTEM— 510(k) K883994

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K883994 for VISTA MR 2055 HP SYSTEM, Substantially Equivalent on 1988-11-21. Applicant: Philips Medical Systems (Cleveland), Inc..

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code LNH
Advisory panel: Radiology
Date received: 1988-09-20
Decision date: 1988-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

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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.