Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K944393 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the o... | 2 | 06/14/2012 | Stryker Instruments Div. of Stryker Corporation |
| T4-Hytrel Zipper Toga Product Usage - The togas are intended to provide a barrier between the op... | 2 | 06/14/2012 | Stryker Instruments Div. of Stryker Corporation |
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