DEVILBISS 9000 SERIES CPAP, MODEL 9001— 510(k) K011229

Name: FDA 510(k) clearance K011229
Creator: U.S. Food and Drug Administration
Published: 2001-07-11

Substantially Equivalent

Sunrise Medical Hhg, Inc.

FDA 510(k) clearance K011229 for DEVILBISS 9000 SERIES CPAP, MODEL 9001, Substantially Equivalent on 2001-07-11. Applicant: Sunrise Medical Hhg, Inc.. Device class: 2.

Clearance details

Applicant: Sunrise Medical Hhg, Inc.
Product code: Code BZD
Device class: Class 2
Regulation: 21 CFR 868.5905
Advisory panel: Anesthesiology
Date received: 2001-04-23
Decision date: 2001-07-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Somerset, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BZD

product code BZD

Death: 4,440
Injury: 53,099
Malfunction: 213,222
Other: 17
Total: 270,778

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.