Curad Kid Size Instant Cold Pack

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

510(k) Number

K920252 ↗

FDA Product Code

IMD

Device Class

Class I

Regulation

21 CFR Part 890.5710

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Curity Vented Dressing System

  Unclassified

  FDA 510(k) K915635 Active Cleared 31 Jan 1992

• Kendall Safetrak Combined Epidural/Spinal Kit

  Class II

  FDA 510(k) K941493 Active Cleared 22 Jun 1994

• Kendall Universal Extension Set

  Class I

  FDA 510(k) K930551 Active Cleared 12 May 1993

• Kendall Home Rx Therapeutic Stocking

  Class II

  FDA 510(k) K925417 Active Cleared 4 Jun 1993

• Curity(R) Calib Tuohy Type Epidur Needle Fix Wing

  Class II

  FDA 510(k) K910791 Active Cleared 17 May 1991

• Curity Pediatric Continuous Caudal Anesthesia Tray

  Class II

  FDA 510(k) K902647 Active Cleared 29 Nov 1990

See all devices from Kendall Healthcare Products Co. Div.Of Tyco Health →