Medical Device Recalls
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1 result found
510(K) Number: K052465 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P and 350P device (SAM 300P and ... | 2 | 07/24/2014 |
FEI # 3004123209 Heartsine Technologies, Limited |
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