DEVILBISS MODEL 7352 SERIES— 510(k) K904766

Substantially Equivalent

Devilbiss Health Care, Inc.

FDA 510(k) clearance K904766 for DEVILBISS MODEL 7352 SERIES, Substantially Equivalent on 1991-03-26. Applicant: Devilbiss Health Care, Inc..

Clearance details

Applicant: Devilbiss Health Care, Inc.
Product code: Code BZD
Advisory panel: Anesthesiology
Date received: 1990-10-22
Decision date: 1991-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, PA, US

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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.