MSI 3002 SERIES BED— 510(k) K881963

Substantially Equivalent

Med Service, Inc.

FDA 510(k) clearance K881963 for MSI 3002 SERIES BED, Substantially Equivalent on 1988-06-28. Applicant: Med Service, Inc..

Clearance details

Applicant: Med Service, Inc.
Product code: Code FNL
Advisory panel: General Hospital
Date received: 1988-05-10
Decision date: 1988-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Batesville, MS, US

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Adverse events under product code FNL

product code FNL

Death: 64
Injury: 728
Malfunction: 10,825
Other: 9
Total: 11,626

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.