THE VERSA-BED— 510(k) K792298

Substantially Equivalent

First & Ten, Inc.

FDA 510(k) clearance K792298 for THE VERSA-BED, Substantially Equivalent on 1979-12-20. Applicant: First & Ten, Inc..

Clearance details

Applicant: First & Ten, Inc.
Product code: Code FNJ
Advisory panel: General Hospital
Date received: 1979-11-13
Decision date: 1979-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FNJ

product code FNJ

Death: 6
Total: 6

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.