Adt Peritoneal Lavage Tray (Disp.)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K800421 ↗

FDA Product Code

GAA

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Ferris Bone Marrow Biopsy-Aspir. Needle

  Class I

  FDA 510(k) K800406 Active Cleared 12 Mar 1980

• A.D.T. Procedures Tray

  Class I

  FDA 510(k) K812297 Active Cleared 28 Sep 1981

• Aspiration Tray W/Ferris Disp. Illinois

  Class I

  FDA 510(k) K800411 Active Cleared 28 Apr 1980

• Adt Bone Mar. Bio/Asp. Tray W/Needle

  Class I

  FDA 510(k) K800408 Active Cleared 28 Apr 1980

• Adt Disposable Thin Needle(Skinny Chiba)

  Class II

  FDA 510(k) K800416 Active Cleared 25 Mar 1980

• Adt Bone Marrow Biopsy-Aspir. Neelde

  Class I

  FDA 510(k) K801753 Active Cleared 20 Aug 1980

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