Medical Device Recalls
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1 result found
510(K) Number: K102639 |
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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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SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA... | 2 | 04/29/2013 | Discus Dental LLC |
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