WILTEK VARICES INJECTION NEEDLE— 510(k) K894868

Substantially Equivalent

Wiltek Medical, Inc.

FDA 510(k) clearance K894868 for WILTEK VARICES INJECTION NEEDLE, Substantially Equivalent on 1989-12-21. Applicant: Wiltek Medical, Inc..

Clearance details

Applicant: Wiltek Medical, Inc.
Product code: Code FBK
Advisory panel: Gastroenterology, Urology
Date received: 1989-07-31
Decision date: 1989-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winston-Salem, NC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FBK

product code FBK

Other: 1
Total: 1

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.