CRAFTMATIC ELECTRIC ADJUSTABLE BED— 510(k) K840787

Name: FDA 510(k) clearance K840787
Creator: U.S. Food and Drug Administration
Published: 1984-06-13

Substantially Equivalent

Contour, Inc.

FDA 510(k) clearance K840787 for CRAFTMATIC ELECTRIC ADJUSTABLE BED, Substantially Equivalent on 1984-06-13. Applicant: Contour, Inc.. Device class: 2.

Clearance details

Applicant: Contour, Inc.
Product code: Code LLI
Device class: Class 2
Regulation: 21 CFR 880.5100
Advisory panel: General Hospital
Date received: 1984-01-20
Decision date: 1984-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLI

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K022387 — CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC2002-09-19

Adverse events under product code LLI

product code LLI

Death: 10
Total: 10

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.