Masterscreen Cpx and Oxycon Cpx

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

510(k) Number

K040698 ↗

FDA Product Code

BZC

Device Class

Class II

Regulation

21 CFR Part 868.1880

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Spiropro SPO2

  Class II

  FDA 510(k) K031515 Active Cleared 14 Nov 2003

• Ball Recording Electrode/Stimulation Probe

  Class II

  FDA 510(k) K030517 Active Cleared 1 Aug 2003

• Masterscreen Pneumo & Masterscope

  Class II

  FDA 510(k) K071753 Active Cleared 14 Aug 2007

• Flowscreen, Flowscreen/Corscreen, Flowscreen CT

  Class II

  FDA 510(k) K080734 Active Cleared 26 Jun 2008

• MasterScreen Paed - Baby Body

  Class II

  FDA 510(k) K081823 Active Cleared 18 May 2009

• Clean Peak Flow Meter

  Class II

  FDA 510(k) K091412 Active Cleared 21 Aug 2009

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