Accupac Custom Skin Scrub Kit

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K861219 ↗

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Accupac Custom Operating Room Procedure-DK876543

  Not classified

  FDA 510(k) K853265 Active Cleared 26 Aug 1985

• Accupac Custom Pack Kerlix Squares

  Unclassified

  FDA 510(k) K861308 Active Cleared 2 May 1986

• Super-Spike Transfer Set

  Class II

  FDA 510(k) K802940 Active Cleared 15 Jan 1981

• Gent-L-Kare Cleansing Enema Set

  Class I

  FDA 510(k) K881218 Active Cleared 28 Jul 1988

• Cook County Hospital Dressing Change Set

  Class I

  FDA 510(k) K843206 Active Cleared 24 May 1985

• Gent-L-Kare Sterile Urinary Leg Bag

  Class II

  FDA 510(k) K881217 Active Cleared 29 Jul 1988

See all devices from Geneva Laboratories, Inc. →