Ice Container I.C.E.

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K792182 ↗

FDA Product Code

IME

Device Class

Class I

Regulation

21 CFR Part 890.5700

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Prebypass Filter Cat.#k-5

  Class II

  FDA 510(k) K803101 Active Cleared 22 Dec 1980

• Vacuum Relief Valve (K760894)

  Class II

  FDA 510(k) K760894 Active Cleared 9 Dec 1976

• Open-Loop Insulin Delivery System

  Class II

  FDA 510(k) K801704 Active Cleared 13 Aug 1980

• Accu-Rynge Pump Sp-250

  Class II

  FDA 510(k) K830389 Active Cleared 12 Sep 1983

• Delivery Tube Set #2226

  Class II

  FDA 510(k) K822761 Active Cleared 30 Sep 1982

• Infusion Pump

  Class II

  FDA 510(k) K832470 Active Cleared 28 Feb 1984

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