WORLDWIDE MEDICAL TECHNOLOGIES I TYPE NEEDLE— 510(k) K980068

Substantially Equivalent

Worldwide Medical Technologies, LLC

FDA 510(k) clearance K980068 for WORLDWIDE MEDICAL TECHNOLOGIES I TYPE NEEDLE, Substantially Equivalent on 1998-01-23. Applicant: Worldwide Medical Technologies, LLC.

Clearance details

Applicant: Worldwide Medical Technologies, LLC
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 1998-01-08
Decision date: 1998-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodbury, CT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KNW

product code KNW

Death: 9
Injury: 965
Malfunction: 10,444
Other: 3
Total: 11,421

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.