PURITAN-BENNETT 840 VENTILATIOR SYSTEM WITH VOLUME VENTILATION PLUS OPTION— 510(k) K021573

Name: FDA 510(k) clearance K021573
Creator: U.S. Food and Drug Administration
Published: 2002-08-13

Substantially Equivalent - Subject to Tracking Reg.

Puritan-Bennett

FDA 510(k) clearance K021573 for PURITAN-BENNETT 840 VENTILATIOR SYSTEM WITH VOLUME VENTILATION PLUS OPTION, Substantially Equivalent - Subject to Tracking Reg. on 2002-08-13. Applicant: Puritan-Bennett. Device class: 2.

Clearance details

Applicant: Puritan-Bennett
Product code: Code CBK
Device class: Class 2
Regulation: 21 CFR 868.5895
Advisory panel: Anesthesiology
Date received: 2002-05-14
Decision date: 2002-08-13
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Special
Location: Carlsbad, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CBK

product code CBK

Death: 736
Injury: 3,628
Malfunction: 98,786
Other: 4
Total: 103,154

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.