Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit)— 510(k) K190026

Name: FDA 510(k) clearance K190026
Creator: U.S. Food and Drug Administration
Published: 2019-08-21

Substantially Equivalent

Teleflex Medical

FDA 510(k) clearance K190026 for Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit), Substantially Equivalent on 2019-08-21. Applicant: Teleflex Medical. Device class: 2.

Clearance details

Applicant: Teleflex Medical
Product code: Code BSP
Device class: Class 2
Regulation: 21 CFR 868.5150
Advisory panel: Anesthesiology
Date received: 2019-01-07
Decision date: 2019-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morrisville, NC, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BSP

product code BSP

Death: 2
Total: 2

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.