Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101490 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| FRAXEL DUAL 1550/1927 Laser System, (FRAXEL SR 1500 DUAL Laser System), for dermatological procedure... | 2 | 04/16/2014 | Solta Medical, Inc. |
| Fraxel re:store® Dual Laser System----a laser surgical instrument for use in general and plastic sur... | 2 | 02/01/2011 | Solta Medical, Inc. |
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