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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K910115
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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BV25 Mobile X-Ray System 2 09/15/2004 Philips Medical Systems Sales & Service Region No. America
BV212 Mobile X-Ray System 2 09/15/2004 Philips Medical Systems Sales & Service Region No. America
BV29 Mobile X-Ray System 2 09/15/2004 Philips Medical Systems Sales & Service Region No. America
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