Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K003614 |
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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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| Light Sheer Desire Diode Laser System with XC Handpiece Accessory options. | 2 | 04/24/2015 |
FEI # 3004135191 Lumenis Limited |
| Lumenis brand LightSheer Pulsed Diode Array Laser System; All serial numbers; Manufactured by RH US... | 2 | 02/23/2006 |
FEI # 2914019 Lumenis Inc. |
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