Sterile Irrigation Trays

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

510(k) Number

K890728 ↗

FDA Product Code

KYZ

Device Class

Class I

Regulation

21 CFR Part 880.6960

Advisory Committee

General Hospital

FDA Decision

SESD Substantially Equivalent — Deferred

• Suture Removal Kit

  Class II

  FDA 510(k) K890729 Active Cleared 17 Apr 1989

• Patient Examination Gloves (Vinyl)

  Class I

  FDA 510(k) K891860 Active Cleared 11 Apr 1989

• Isosafe Earloop Procedure Mask (Blue, Yellow)

  Class II

  FDA 510(k) K972849 Active Cleared 28 May 1998

• Cypress Medical Products Catheter (Insertion) Tray

  Class II

  FDA 510(k) K950092 Active Cleared 27 Feb 1995

• Tracheostomy Care and Cleaning Kits

  Class II

  FDA 510(k) K890726 Active Cleared 10 Mar 1989

• Cypress Medical Products Catheter (Insertion) Tray/with Out Catheter

  Class II

  FDA 510(k) K950109 Active Cleared 27 Feb 1995

See all devices from Cypress Medical Products, Ltd. →