MSI 2005 SERIES BED— 510(k) K881962

Name: FDA 510(k) clearance K881962
Creator: U.S. Food and Drug Administration
Published: 1988-06-03

Substantially Equivalent

Med Service, Inc.

FDA 510(k) clearance K881962 for MSI 2005 SERIES BED, Substantially Equivalent on 1988-06-03. Applicant: Med Service, Inc.. Device class: 1.

Clearance details

Applicant: Med Service, Inc.
Product code: Code FNJ
Device class: Class 1
Regulation: 21 CFR 880.5120
Advisory panel: General Hospital
Date received: 1988-05-10
Decision date: 1988-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Batesville, MS, US

Download summary PDF View on FDA.gov ↗

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K884542 — SIC 3999 FOLDING ADJUSTABLE HOSPITAL BED1988-11-21
K881725 — ENVIROTENT (BED)1988-11-08

More clearances from Med Service, Inc.

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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 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.