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