MSI 5000 SERIES BED— 510(k) K881965

Name: FDA 510(k) clearance K881965
Creator: U.S. Food and Drug Administration
Published: 1988-05-31

Substantially Equivalent

Med Service, Inc.

FDA 510(k) clearance K881965 for MSI 5000 SERIES BED, Substantially Equivalent on 1988-05-31. Applicant: Med Service, Inc.. Device class: 2.

Clearance details

Applicant: Med Service, Inc.
Product code: Code FNL
Device class: Class 2
Regulation: 21 CFR 880.5100
Advisory panel: General Hospital
Date received: 1988-05-10
Decision date: 1988-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Batesville, MS, US

Download summary PDF View on FDA.gov ↗

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K881960 — MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-741988-11-01
K881961 — MSI STANDARD BED MODELS: L1097-64 AND L1085-641988-11-01
K881782 — MSI 4000 SERIES BED1988-07-12
K881963 — MSI 3002 SERIES BED1988-06-28
K881964 — MSI 3003 SERIES BED1988-06-28

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.