Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K070596 |
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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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| Pediatric Laryngo-Tracheal Atomizer Device without syringe, LATEX FREE For Single patient Use Only ... | 2 | 11/16/2009 |
FEI # 3020651884 Sharn, Inc. |
| Nasal Mucosal Atomizer Device without syringe, LATEX FREE For Single Patient Use Only Packaged Clean... | 2 | 11/16/2009 |
FEI # 3020651884 Sharn, Inc. |
| Nasal Mucosal Atomizer Device with syringe, LATEX FREE For Single Patient Use Only Packaged Clean -N... | 2 | 11/16/2009 |
FEI # 3020651884 Sharn, Inc. |
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