SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM— 510(k) K133763

Substantially Equivalent

Medi-Globe Corporation

FDA 510(k) clearance K133763 for SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM, Substantially Equivalent on 2014-05-15. Applicant: Medi-Globe Corporation.

Clearance details

Applicant: Medi-Globe Corporation
Product code: Code FCG
Advisory panel: Gastroenterology, Urology
Date received: 2013-12-11
Decision date: 2014-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tempe, AZ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FCG

product code FCG

Death: 13
Injury: 576
Malfunction: 1,966
Total: 2,555

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.