TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060— 510(k) K050926

Substantially Equivalent

Idev Technologies, Inc.

FDA 510(k) clearance K050926 for TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060, Substantially Equivalent on 2005-05-09. Applicant: Idev Technologies, Inc..

Clearance details

Applicant: Idev Technologies, Inc.
Product code: Code MMX
Advisory panel: Cardiovascular
Date received: 2005-04-13
Decision date: 2005-05-09
Decision: Substantially Equivalent
Clearance type: Special
Location: Houston, TX, US

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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.