Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032949 |
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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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| Dixtal Handheld Pulse Oximetry Model 512 Catalog Number: 9100-00 | 2 | 12/09/2010 |
FEI # 3006891479 Dixtal Medical, Inc. |
| Dixtal Handheld Pulse Oximetry Model 513 Catalog Number: 9300-00 | 2 | 12/09/2010 |
FEI # 3006891479 Dixtal Medical, Inc. |
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