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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K071800
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Product Description
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FDA Recall
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Philips Avalon Fetal Monitor FM 20 Catalog Number: M2702A. 2 12/17/2009 Philips Healthcare Inc.
Philips Avalon Fetal Monitor FM 30 Catalog Number: M2703A. 2 12/17/2009 Philips Healthcare Inc.
Philips Avalon Fetal Monitor FM20; Model Number: M2702A. 2 06/26/2009 Philips Healthcare Inc.
Philips Avalon Fetal Monitor FM30; Model Number: M2703A. 2 06/26/2009 Philips Healthcare Inc.
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