K932292

Substantially Equivalent

AUTOTUNE DEVICE (ATD II) FOR PICKER MRI SYSTEMS

Applicant: Medrad, Inc.
Product code: LNH
Advisory panel: Radiology
Date received: 1993-05-10
Decision date: 1993-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianola, PA, US

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.