ULDALL SUBCLAVIAN CANNULA SC-100— 510(k) K791308

Name: FDA 510(k) clearance K791308
Creator: U.S. Food and Drug Administration
Published: 1979-08-03

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K791308 for ULDALL SUBCLAVIAN CANNULA SC-100, Substantially Equivalent on 1979-08-03. Applicant: Vas-Cath of Canada , Ltd.. Device class: 2.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code FIQ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1979-07-16
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K844692 — PEDIATRIC SIZED HEMOCATH CATHETER1985-01-18
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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.