Cardiac Cath or Angiographic Trays

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

510(k) Number

K932218 ↗

FDA Product Code

DQO

Device Class

Class II

Regulation

21 CFR Part 870.1200

Advisory Committee

Cardiovascular

FDA Decision

SEKD

• Ampco Skin Scrub Tray

  Class I

  FDA 510(k) K802375 Active Cleared 10 Oct 1980

• Dressing Change Tray-Medium

  Class II

  FDA 510(k) K802954 Active Cleared 17 Dec 1980

• Ampco Opthalmic Tray

  Class II

  FDA 510(k) K842983 Active Cleared 22 May 1985

• C-Section, Labor & Delivery Trays (Packs)

  Class II

  FDA 510(k) K932216 Active Cleared 19 Apr 1994

• Neurological or Crani Trays (Packs)

  Class II

  FDA 510(k) K932221 Active Cleared 19 Mar 1997

• Lap Choly Trays (Packs)

  Class II

  FDA 510(k) K932220 Active Cleared 27 Sep 1993

See all devices from Associated Medical Products Co. →