SUBCLAVIAN HEMODIALYSIS CATHETER— 510(k) K884322

Name: FDA 510(k) clearance K884322
Creator: U.S. Food and Drug Administration
Published: 1989-04-25

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K884322 for SUBCLAVIAN HEMODIALYSIS CATHETER, Substantially Equivalent on 1989-04-25. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1988-10-14
Decision date: 1989-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sandy, UT, US

Download summary PDF View on FDA.gov ↗

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