VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM— 510(k) K041321

Substantially Equivalent

Richard Wolf Medical Instruments Corp.

FDA 510(k) clearance K041321 for VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM, Substantially Equivalent on 2004-07-09. Applicant: Richard Wolf Medical Instruments Corp..

Clearance details

Applicant: Richard Wolf Medical Instruments Corp.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 2004-05-18
Decision date: 2004-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vernon Hills, IL, US

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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.