PLEUR-EVAC(R) ADULT/PEDI DUAL COLL CHEST DRAIN SYS— 510(k) K924337

Substantially Equivalent

Deknatel, Inc.

FDA 510(k) clearance K924337 for PLEUR-EVAC(R) ADULT/PEDI DUAL COLL CHEST DRAIN SYS, Substantially Equivalent on 1993-07-28. Applicant: Deknatel, Inc..

Clearance details

Applicant: Deknatel, Inc.
Product code: Code GCX
Advisory panel: General Hospital
Date received: 1992-08-27
Decision date: 1993-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose-Heredia, CR

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Adverse events under product code GCX

product code GCX

Death: 9
Malfunction: 592
Other: 2
Total: 603

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.