Medical Device Recalls
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1 result found
510(K) Number: K083500 |
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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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| Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K100... | 2 | 05/21/2019 | Dornier Medtech America, Inc. |
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