DUAL LUMEN MIDLINE CATHETER— 510(k) K010349

Substantially Equivalent

Catheter Innovations, Inc.

FDA 510(k) clearance K010349 for DUAL LUMEN MIDLINE CATHETER, Substantially Equivalent on 2001-02-28. Applicant: Catheter Innovations, Inc..

Clearance details

Applicant: Catheter Innovations, Inc.
Product code: Code LJS
Advisory panel: General Hospital
Date received: 2001-02-05
Decision date: 2001-02-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Salt Lake City, UT, US

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Adverse events under product code LJS

product code LJS

Death: 31
Injury: 2,791
Malfunction: 18,374
Other: 5
Total: 21,201

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.