Modification of Kendall Curasorb Calcium Alginate Wound Dressing

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

510(k) Number

K933689 ↗

FDA Product Code

KMF

Device Class

Class I

Regulation

21 CFR Part 880.5090

Advisory Committee

General Hospital

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

• Curad Kid Size Instant Cold Pack

  Class I

  FDA 510(k) K920252 Active Cleared 11 Feb 1992

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

  Class II

  FDA 510(k) K910791 Active Cleared 17 May 1991

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