K062725

Substantially Equivalent

MAXIFLEX-SEMI FLEX SCOPE

Applicant: Technology Delivery Systems, Inc.
Product code: FGB
Advisory panel: Gastroenterology, Urology
Date received: 2006-09-13
Decision date: 2006-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Adverse events under product code FGB

product code FGB

Death: 6
Injury: 552
Malfunction: 3,922
Other: 1
Total: 4,481

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.