TROCAR CATHETER/THORACIC CATHETER— 510(k) K792202

Name: FDA 510(k) clearance K792202
Creator: U.S. Food and Drug Administration
Published: 1979-11-20

Substantially Equivalent

Portex, Inc.

FDA 510(k) clearance K792202 for TROCAR CATHETER/THORACIC CATHETER, Substantially Equivalent on 1979-11-20. Applicant: Portex, Inc.. Device class: 2.

Clearance details

Applicant: Portex, Inc.
Product code: Code DWF
Device class: Class 2
Regulation: 21 CFR 870.4210
Advisory panel: Cardiovascular
Date received: 1979-11-02
Decision date: 1979-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DWF

product code DWF

Death: 106
Injury: 386
Malfunction: 2,323
Total: 2,815

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.