Leg Bag Extension Tube

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K802606 ↗

FDA Product Code

KNX

Device Class

Class II

Regulation

21 CFR Part 876.5250

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Ampco Skin Scrub Tray

  Class I

  FDA 510(k) K802375 Active Cleared 10 Oct 1980

• Dressing Change Tray-Medium

  Class II

  FDA 510(k) K802954 Active Cleared 17 Dec 1980

• Ampco Opthalmic Tray

  Class II

  FDA 510(k) K842983 Active Cleared 22 May 1985

• C-Section, Labor & Delivery Trays (Packs)

  Class II

  FDA 510(k) K932216 Active Cleared 19 Apr 1994

• Neurological or Crani Trays (Packs)

  Class II

  FDA 510(k) K932221 Active Cleared 19 Mar 1997

• Lap Choly Trays (Packs)

  Class II

  FDA 510(k) K932220 Active Cleared 27 Sep 1993

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