Medical Device Recalls
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1 result found
510(K) Number: K022637 |
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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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| BD K-3000 Microkeratome Blade REF 378607 | 2 | 03/12/2003 | BD Opthalmic Systems |
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