PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST— 510(k) K882223

Substantially Equivalent

Deknatel, Inc.

FDA 510(k) clearance K882223 for PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST, Substantially Equivalent on 1988-08-16. Applicant: Deknatel, Inc..

Clearance details

Applicant: Deknatel, Inc.
Product code: Code KDQ
Advisory panel: General Hospital
Date received: 1988-05-26
Decision date: 1988-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, US

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Adverse events under product code KDQ

product code KDQ

Death: 8
Malfunction: 637
Total: 645

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.