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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K010413
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Pulsox-3iA. LCD, Sp02, PR, Pulse strength bar, motion artifact, low battery message, error message,... 2 07/20/2004 FEI # 1000136179
Minolta Corp
Pulsox-3Si. LCD, SpO2, PR, Pulse strength bar, Motion artifact, Low battery message, Error message,... 2 07/20/2004 FEI # 1000136179
Minolta Corp
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