K033188

Substantially Equivalent

TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050

Applicant: Idev Technologies, Inc.
Product code: MMX
Advisory panel: Cardiovascular
Date received: 2003-10-01
Decision date: 2003-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Adverse events under product code MMX

product code MMX

Death: 3
Total: 3

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.