HILL-ROM VIA STRETCHER (P1300 - P1303)— 510(k) K922808

Substantially Equivalent

Hill-Rom, Inc.

FDA 510(k) clearance K922808 for HILL-ROM VIA STRETCHER (P1300 - P1303), Substantially Equivalent on 1993-03-31. Applicant: Hill-Rom, Inc..

Clearance details

Applicant: Hill-Rom, Inc.
Product code: Code FPO
Advisory panel: General Hospital
Date received: 1992-06-10
Decision date: 1993-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Batesville, TN, US

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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.