DOUBLE LUMEN SUBCLAVIAN CATHETER— 510(k) K823135

Name: FDA 510(k) clearance K823135
Creator: U.S. Food and Drug Administration
Published: 1983-03-07

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K823135 for DOUBLE LUMEN SUBCLAVIAN CATHETER, Substantially Equivalent on 1983-03-07. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1982-10-28
Decision date: 1983-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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