UltraCath Continuous Nerve block Catheter— 510(k) K162522

Substantially Equivalent

Teleflexmedical, Inc.

FDA 510(k) clearance K162522 for UltraCath Continuous Nerve block Catheter, Substantially Equivalent on 2017-03-17. Applicant: Teleflexmedical, Inc..

Clearance details

Applicant: Teleflexmedical, Inc.
Product code: Code BSO
Advisory panel: Anesthesiology
Date received: 2016-09-09
Decision date: 2017-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morrisville, NC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BSO

product code BSO

Malfunction: 688
Total: 688

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.