Medical Device Recalls
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1 result found
510(K) Number: K924226 |
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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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Integra Ojemann Cortical Stimulator; Product / Catalogue No: OCS2. Intended for intraoperative c... | 2 | 04/01/2013 | Integra Burlington MA, Inc. |
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