K062097

Substantially Equivalent

VERESS CANNULA AND MODULAR VERESS CANNULA

Applicant: PAJUNK GmbH Medizintechnologie
Product code: HET
Advisory panel: Obstetrics/Gynecology
Date received: 2006-07-24
Decision date: 2006-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geisingen, DE

Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

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.