Medical Device Recalls
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1 result found
510(K) Number: K003759 |
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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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| Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: ... | 2 | 09/26/2016 | Spiegelberg Gmbh & Co. KG |
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