Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K921860 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Burette Set w/150 ml Burette w/15 um filter & Ultrasite inj site, Ultrasite inj site, 88 in US1540. ... | 2 | 09/23/2008 |
FEI # 2523676 B. Braun Medical, Inc. |
| Burette Set w/150 ml burette w/15 um filter & inj site, inj site, with automatic shutoff 87 in. Item... | 2 | 09/23/2008 |
FEI # 2523676 B. Braun Medical, Inc. |
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