Medical Device Recalls
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1 result found
510(K) Number: K991086 |
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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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| 8400 Capnocheck Capnometer uses power cord 8404 (Electri-Cord Manufacturing, 312 E. Main St, Westfie... | 2 | 03/02/2010 |
FEI # 2183502 Smiths Medical PM, Inc. |
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