ARGON DUAL LUMEN HEMODIALYSIS, CATHETER— 510(k) K842039

Name: FDA 510(k) clearance K842039
Creator: U.S. Food and Drug Administration
Published: 1985-01-29

Substantially Equivalent

Argon Medical Corp.

FDA 510(k) clearance K842039 for ARGON DUAL LUMEN HEMODIALYSIS, CATHETER, Substantially Equivalent on 1985-01-29. Applicant: Argon Medical Corp.. Device class: 2.

Clearance details

Applicant: Argon Medical Corp.
Product code: Code KNZ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1984-05-21
Decision date: 1985-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Athens, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNZ

view all

K844612 — ACUTE HEMODIALYSIS TRAYS1984-12-17
K842864 — VACCESS FEMORAL CANNULA1984-08-08
K842416 — DUO FLOW CATHETER-MC 541984-07-26
K841530 — DOUBLE LUMEN SUBLCAVIAN-FEMORAL1984-06-25
K841119 — TOPS DISPOS. INFUSION SET/HEMODIALYSIS1984-04-20

More clearances from Argon Medical Corp.

view all

K904994 — CLOSED SYSTEM FLUSH SET1991-01-15
K895511 — CATHETER BALLOON DILATOR PRESSURE GAUGE1990-02-28
K894157 — OBTURATOR1989-09-28
K891022 — INTRODUCER FOR PTCA GUIDING CATHETERS1989-05-19
K884375 — TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER1989-01-11

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