VACCESS TM 4006— 510(k) K853283

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K853283 for VACCESS TM 4006, Substantially Equivalent on 1985-08-22. Applicant: Vas-Cath of Canada , Ltd.. Device class: 2.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1985-08-05
Decision date: 1985-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, L5a 3v3, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code LFJ

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K925819 — AKCESS0CATH KIT1994-08-02
K925818 — AKCESS-CATH1994-04-05
K913468 — ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAY1994-03-24
K920634 — SPLITTABLE SHEATH INTRODUCER SET1994-01-14

More clearances from Vas-Cath of Canada , Ltd.

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
K863982 — VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY1986-10-24

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