PURITAN-BENNETT COMPANION 320 I/E BI-LEVEL RESPIRATORY SYSTEM— 510(k) K935784

Substantially Equivalent

Puritan-Bennett

FDA 510(k) clearance K935784 for PURITAN-BENNETT COMPANION 320 I/E BI-LEVEL RESPIRATORY SYSTEM, Substantially Equivalent on 1994-07-13. Applicant: Puritan-Bennett.

Clearance details

Applicant: Puritan-Bennett
Product code: Code BZD
Advisory panel: Anesthesiology
Date received: 1993-12-06
Decision date: 1994-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, 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.