Alba Dry Burn Pad

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K850881 ↗

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Procedure & Recovery Patient Suit

  Class II

  FDA 510(k) K803171 Active Cleared 4 Mar 1981

• Alba Dry Burn Dressing

  Class I

  FDA 510(k) K850904 Active Cleared 17 Apr 1985

• Alba Health Care Non-Adhering Dressing

  Unclassified

  FDA 510(k) K850241 Active Cleared 12 Mar 1985

• Alba Health Care Iodoform Packing Strip

  Not classified

  FDA 510(k) K864689 Active Cleared 20 Jan 1987

• Sterile Orthopedic Stockinette

  Class I

  FDA 510(k) K812904 Active Cleared 18 Jan 1982

• Alba Health Care Plain Packing Strip

  Unclassified

  FDA 510(k) K861154 Active Cleared 15 Apr 1986

See all devices from Alba Health Care →