Medical Device Recalls
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1 result found
510(K) Number: K990323 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Poly Stim II Nerve Stimulator 8 inch for use with Stryker Pain Pump, REF 550-100, Rx, Sterile, Di... | 2 | 09/03/2010 | Stryker Instruments Div. of Stryker Corporation |
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