Mini Ox III Oxygen Monitor

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

510(k) Number

K833326 ↗

FDA Product Code

BXL

Device Class

Class I

Regulation

21 CFR Part 868.1030

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Miniox IV Portable Pulse Oximeter

  Class II

  FDA 510(k) K874132 Active Cleared 19 Jan 1988

• Model M25RL, (Crc) Oxygen Analyzer

  Class II

  FDA 510(k) K790785 Active Cleared 27 Apr 1979

• Oxygen Analyzer, Model M25RA & M25RAD

  Class II

  FDA 510(k) K782062 Active Cleared 15 Feb 1979

• Miniox 100 Pulse Oximeter

  Class II

  FDA 510(k) K862798 Active Cleared 28 Aug 1986

• Minico

  Class II

  FDA 510(k) K781746 Active Cleared 5 Dec 1978

• Miniox V Pulse Oximeter

  Class II

  FDA 510(k) K905310 Active Cleared 28 May 1991

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