CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED— 510(k) K962250

Name: FDA 510(k) clearance K962250
Creator: U.S. Food and Drug Administration
Published: 1996-10-21

Substantially Equivalent

Carroll Healthcare, Inc.

FDA 510(k) clearance K962250 for CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED, Substantially Equivalent on 1996-10-21. Applicant: Carroll Healthcare, Inc.. Device class: 2.

Clearance details

Applicant: Carroll Healthcare, Inc.
Product code: Code FNL
Device class: Class 2
Regulation: 21 CFR 880.5100
Advisory panel: General Hospital
Date received: 1996-06-12
Decision date: 1996-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code FNL

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K202964 — iBed Wireless with iBed Mobile2021-06-18
K103536 — IBED WIRELESS WITH IBED AWARENESS2010-12-16
K982783 — VAIL 1000 ENCLOSED BED1998-10-05
K974296 — MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED1998-01-06
K974254 — BENEFIT B3--- SERIES1997-12-16

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.