VACCESS FEMORAL CANNULA— 510(k) K842864

Name: FDA 510(k) clearance K842864
Creator: U.S. Food and Drug Administration
Published: 1984-08-08

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K842864 for VACCESS FEMORAL CANNULA, Substantially Equivalent on 1984-08-08. Applicant: Vas-Cath of Canada , Ltd.. Device class: 2.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code KNZ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1984-07-23
Decision date: 1984-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K842416 — DUO FLOW CATHETER-MC 541984-07-26
K841530 — DOUBLE LUMEN SUBLCAVIAN-FEMORAL1984-06-25
K841119 — TOPS DISPOS. INFUSION SET/HEMODIALYSIS1984-04-20

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K871487 — VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH1987-06-12
K871488 — VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH1987-06-12
K863982 — VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY1986-10-24

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