VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY— 510(k) K863982

Name: FDA 510(k) clearance K863982
Creator: U.S. Food and Drug Administration
Published: 1986-10-24

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K863982 for VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY, Substantially Equivalent on 1986-10-24. Applicant: Vas-Cath of Canada , Ltd.. Device class: 1.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code JCY
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1986-10-14
Decision date: 1986-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, L5a 3v3, CA

Download summary PDF View on FDA.gov ↗

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K831453 — SILCATH CENTRAL CATHETER TRAY W/18 GA1983-07-28
K831451 — SILCATH CENTRAL CATHETER TRAY SIZE-1983-06-08
K822096 — CHEMOTHERAPY INFUSION CATHETER1983-04-12

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K875188 — LUER LOCK CONNECTORS / RIDIG P.V.C.1988-03-02
K871817 — VAS-CATH PERITONEAL DIALYSIS CATHETER1987-07-16
K871487 — VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH1987-06-12
K871488 — VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH1987-06-12
K853283 — VACCESS TM 40061985-08-22

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