Vas-Cath Pericardiocentesis Catheter, Set & Tray

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K863982 ↗

FDA Product Code

JCY

FDA applicant

Vas-Cath of Canada , Ltd.

Device Class

Class I

Regulation

21 CFR Part 878.4200

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Vaccess TM 4006

  Class II

  FDA 510(k) K853283 Active Cleared 22 Aug 1985

• Vas-Cath Peritoneal Dialysis Catheter

  Class II

  FDA 510(k) K871817 Active Cleared 16 Jul 1987

• Vas-Cath Parallel Dual Luman Jugular Cannual Cath

  Class II

  FDA 510(k) K844336 Active Cleared 13 Mar 1985

• Parallel Dual Lumen Subclavian Cannula

  Class II

  FDA 510(k) K834358 Active Cleared 2 Apr 1984

• Evans, Vas-Cath Epidural Needle & Catheter

  Class II

  FDA 510(k) K850009 Active Cleared 13 May 1985

• Vas-Cath Permanent Dual Lumen Hemodialysis Cath

  Class II

  FDA 510(k) K871488 Active Cleared 12 Jun 1987

See all devices from Vas-Cath of Canada, Ltd. →