Medical Device Recalls
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1 result found
510(K) Number: K993154 |
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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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| A.R.C. Laser Photolysis Probe/Handpiece | 2 | 07/03/2003 |
FEI # 3003111512 A.R.C. Laser Corp |
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