Medical Device Recalls
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1 result found
510(K) Number: K042165 |
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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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Titan XL Handpiece Infrared Therapeutic Heating Lamp, Manufactured by Cutera Inc, Brisbane, CA Infr... | 2 | 11/09/2010 | Cutera Inc |
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