Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K961442 |
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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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| Urethral Catheter Tray catalog# 900-278 | 2 | 03/21/2012 | Customed, Inc |
| Universal drainage kit, catalog# 900-032 | 2 | 03/21/2012 | Customed, Inc |
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