Right Atrial Catheter

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

510(k) Number

K930630 ↗

FDA Product Code

LJS

Device Class

Class II

Regulation

21 CFR Part 880.5970

Advisory Committee

General Hospital

FDA Decision

SN

• Tenckhoff Peritoneal Dialysis Kit

  Class II

  FDA 510(k) K902203 Active Cleared 1 Aug 1990

• Fc-101 Femoral Catheter Guide Wire

  Class II

  FDA 510(k) K891764 Active Cleared 7 Apr 1989

• Dual Lumen Sub-Clavian Catheters Dlsc 600S & 800S

  Class II

  FDA 510(k) K900803 Active Cleared 25 Apr 1990

• Vessel Dilators

  Class II

  FDA 510(k) K910502 Active Cleared 29 Apr 1991

• Y Adaptor

  Class II

  FDA 510(k) K910321 Active Cleared 16 Apr 1991

• Introducer Needles

  Class II

  FDA 510(k) K910641 Active Cleared 29 Apr 1991

See all devices from Akcess Medical Products, Inc. →