KENDALL-LTP TURNER SAVE-A-LINE— 510(k) K003511

Name: FDA 510(k) clearance K003511
Creator: U.S. Food and Drug Administration
Published: 2001-01-24

Substantially Equivalent

The Ludlow Company LP

FDA 510(k) clearance K003511 for KENDALL-LTP TURNER SAVE-A-LINE, Substantially Equivalent on 2001-01-24. Applicant: The Ludlow Company LP. Device class: 1.

Clearance details

Applicant: The Ludlow Company LP
Product code: Code FRP
Device class: Class 1
Regulation: 21 CFR 880.5680
Advisory panel: General Hospital
Date received: 2000-11-14
Decision date: 2001-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicopee, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.