Central Venous Catheter W/Big-Gard

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

510(k) Number

K841828 ↗

FDA Product Code

DQY

Device Class

Class II

Regulation

21 CFR Part 870.1250

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Stopcock, Three Way

  Class II

  FDA 510(k) K791107 Active Cleared 22 Jun 1979

• Tygon Pac-Stopcocks

  Class II

  FDA 510(k) K770708 Active Cleared 8 Jun 1977

• Norton Manifold

  Class II

  FDA 510(k) K820864 Active Cleared 15 Apr 1982

• Tygon Pac-Monitoring Lines & Fluid Admin

  Class II

  FDA 510(k) K770916 Active Cleared 17 Jun 1977

• Percutaneous Catheter Introducer Adapter

  Class II

  FDA 510(k) K800621 Active Cleared 24 Apr 1980

• Venous M/a Internal Jugular Kit

  Class II

  FDA 510(k) K800620 Active Cleared 24 Apr 1980

See all devices from Norton Performance Plastics Corp. →