Disposable Procedural Trays #ck-Xxxxx (Various)

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

510(k) Number

K902441 ↗

FDA Product Code

KDD

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SEKD

• Ck 4900 Series, Gown and Towel Pak

  Class II

  FDA 510(k) K874760 Active Cleared 10 Dec 1987

• CK10000 Series Pouch & Bags Etc.

  Class II

  FDA 510(k) K834558 Active Cleared 5 Sep 1984

• ALP VasQcare Take Home System

  Class II

  FDA 510(k) K151158 Active Cleared 10 Dec 2015

• Currie Medical Reprocessed Alp Calf/Thigh/Foot Compression Sleeve (All Sizes)

  Class II

  FDA 510(k) K140092 Active Cleared 16 Apr 2014

• CK 1600 Series Towels

  Class II

  FDA 510(k) K872395 Active Cleared 2 Jul 1987

• Cms 2000 Series Tpn Kits

  Class I

  FDA 510(k) K831964 Active Cleared 11 Aug 1983

See all devices from Currie Medical Specialties, Inc. →