VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY— 510(k) K844982

Name: FDA 510(k) clearance K844982
Creator: U.S. Food and Drug Administration
Published: 1985-01-18

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K844982 for VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY, Substantially Equivalent on 1985-01-18. Applicant: Vas-Cath of Canada , Ltd.. Device class: 2.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code CAZ
Device class: Class 2
Regulation: 21 CFR 868.5140
Advisory panel: Anesthesiology
Date received: 1984-12-26
Decision date: 1985-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, L5a 3v3, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAZ

view all

K222341 — Arrow 0.2 Micron Flat Filter, GVS2023-02-13
K210983 — BD Epilor Syringe2022-05-19
K201356 — Plastic LOR Syringe2021-02-12
K202699 — E-Cath STIM acc. Tsui2020-12-29
K190345 — VPC2019-05-16

More clearances from Vas-Cath of Canada , Ltd.

view all

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

Adverse events under product code CAZ

product code CAZ

Injury: 145
Malfunction: 942
Other: 1
Total: 1,088

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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