ANCHOR GUIDE LESION LOCALIZATION DEVICE; ANCOR GUIDE HOLDER; RF GENERATOR CABLE— 510(k) K012023

Substantially Equivalent

Senorx, Inc.

FDA 510(k) clearance K012023 for ANCHOR GUIDE LESION LOCALIZATION DEVICE; ANCOR GUIDE HOLDER; RF GENERATOR CABLE, Substantially Equivalent on 2001-09-12. Applicant: Senorx, Inc..

Clearance details

Applicant: Senorx, Inc.
Product code: Code KNW
Advisory panel: Gastroenterology, Urology
Date received: 2001-06-28
Decision date: 2001-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aliso Viejo, CA, 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.