K923730

Substantially Equivalent

MODEL 561 C-ARM PROCEDURES STRETCHER

Applicant: Midmark Corp.
Product code: FPO
Advisory panel: General Hospital
Date received: 1992-07-27
Decision date: 1994-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Versailles, OH, US

Adverse events under product code FPO

product code FPO

Death: 29
Injury: 254
Malfunction: 5,054
Other: 10
Total: 5,347

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.